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Artigo de periodico
Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome (1995)
Spinelli, M; Rocha, A C O; Giacheti, C M; Richieri-Costa, A
Source: American Journal of Medical Genetics (Neuropsychiatric Genetics). Unidade: HRAC
Assunto: FONOAUDIOLOGIA
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ABNT
SPINELLI, M et al. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), v. 60, p. 39-43, 1995Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320600108. Acesso em: 19 abr. 2024.
APA
Spinelli, M., Rocha, A. C. O., Giacheti, C. M., & Richieri-Costa, A. (1995). Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), 60, 39-43. doi:10.1002/ajmg.1320600108
NLM
Spinelli M, Rocha ACO, Giacheti CM, Richieri-Costa A. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome [Internet]. American Journal of Medical Genetics (Neuropsychiatric Genetics). 1995 ; 60 39-43.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320600108
Vancouver
Spinelli M, Rocha ACO, Giacheti CM, Richieri-Costa A. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome [Internet]. American Journal of Medical Genetics (Neuropsychiatric Genetics). 1995 ; 60 39-43.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320600108
Artigo de periodico
Waardenburg syndrome: clinical differentiation between types I and II (2003)
Pardono, Eliete; Bever, Yolande van; Ende, Jenneke van den; Havrenne, Poti Chimetta; Iughetti, Paula; Maestrelli, Sylvia Regina Pedrosa; Costa Filho, Orozimbo Alves; Richieri-Costa, Antonio; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidades: FOB, HRAC, IB
Assunto: ANORMALIDADES CRANIOFACIAIS
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ABNT
PARDONO, Eliete et al. Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, v. 117A, n. 3, p. 223-235, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10193. Acesso em: 19 abr. 2024.
APA
Pardono, E., Bever, Y. van, Ende, J. van den, Havrenne, P. C., Iughetti, P., Maestrelli, S. R. P., et al. (2003). Waardenburg syndrome: clinical differentiation between types I and II. American Journal of Medical Genetics, 117A( 3), 223-235. doi:10.1002/ajmg.a.10193
NLM
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Vancouver
Pardono E, Bever Y van, Ende J van den, Havrenne PC, Iughetti P, Maestrelli SRP, Costa Filho OA, Richieri-Costa A, Frota-Pessoa O, Otto PA. Waardenburg syndrome: clinical differentiation between types I and II [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 3): 223-235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.10193
Trabalho de evento-resumo
Vici's syndrome associated to cleft palate: clinical report on a brazilian boy (2013)
Siemann, M. E.; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio ; Maximino, Luciana Paula
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRAC, FOB
Subjects: FISSURA LÁBIOPALATINA, GENÉTICA
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ABNT
SIEMANN, M. E. et al. Vici's syndrome associated to cleft palate: clinical report on a brazilian boy. 2013, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013. Disponível em: https://repositorio.usp.br/directbitstream/28991ba9-2f6d-4e9e-b359-06d737d5e2bf/2514417.pdf. Acesso em: 19 abr. 2024.
APA
Siemann, M. E., Zechi-Ceide, R. M., Nakata, N. M. K., Pittoli, S. V. P., Guion-Almeida, M. L., Richieri-Costa, A., & Maximino, L. P. (2013). Vici's syndrome associated to cleft palate: clinical report on a brazilian boy. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/28991ba9-2f6d-4e9e-b359-06d737d5e2bf/2514417.pdf
NLM
Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Guion-Almeida ML, Richieri-Costa A, Maximino LP. Vici's syndrome associated to cleft palate: clinical report on a brazilian boy [Internet]. Anais. 2013 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/28991ba9-2f6d-4e9e-b359-06d737d5e2bf/2514417.pdf
Vancouver
Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Guion-Almeida ML, Richieri-Costa A, Maximino LP. Vici's syndrome associated to cleft palate: clinical report on a brazilian boy [Internet]. Anais. 2013 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/28991ba9-2f6d-4e9e-b359-06d737d5e2bf/2514417.pdf
Artigo de periodico
Variable phenotypic manifestations of a K44N mutation in the TGIF gene (2008)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: Brain & Development. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, GENES
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ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, v. 30, n. 3, p. 203-205, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.braindev.2007.07.012. Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2008). Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, 30( 3), 203-205. doi:10.1016/j.braindev.2007.07.012
NLM
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Vancouver
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Artigo de periodico
Variable expressivity of the acheiropodia gene (1983)
Grimaldi, Angela; Masiero, D; Richieri-Costa, Antonio; Maia, A. Freire
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES CONGÊNITAS, GENES, FENÓTIPOS
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ABNT
GRIMALDI, Angela et al. Variable expressivity of the acheiropodia gene. American Journal of Medical Genetics, v. 16, n. 4, p. 631-634, 1983Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320160420. Acesso em: 19 abr. 2024.
APA
Grimaldi, A., Masiero, D., Richieri-Costa, A., & Maia, A. F. (1983). Variable expressivity of the acheiropodia gene. American Journal of Medical Genetics, 16( 4), 631-634. doi:10.1002/ajmg.1320160420
NLM
Grimaldi A, Masiero D, Richieri-Costa A, Maia AF. Variable expressivity of the acheiropodia gene [Internet]. American Journal of Medical Genetics. 1983 ; 16( 4): 631-634.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320160420
Vancouver
Grimaldi A, Masiero D, Richieri-Costa A, Maia AF. Variable expressivity of the acheiropodia gene [Internet]. American Journal of Medical Genetics. 1983 ; 16( 4): 631-634.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320160420
Artigo de periodico
Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures (2005)
Guerra, Dania; Sanchez, Otto; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
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ABNT
GUERRA, Dania e SANCHEZ, Otto e RICHIERI-COSTA, Antonio. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 377-380, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30665. Acesso em: 19 abr. 2024.
APA
Guerra, D., Sanchez, O., & Richieri-Costa, A. (2005). Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, 136( 4), 377-380. doi:10.1002/ajmg.a.30665
NLM
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Vancouver
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Trabalho de evento-resumo
Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations (2009)
Zechi-Ceide, Roseli Maria ; Guion-Almeida, Maria Leine; Oliveira, N. A. J; Richieri-Costa, Antonio ; Passos-Bueno, Maria Rita
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: SÍNDROMES OROFACIODIGITAIS, FENÓTIPOS, MUTAÇÃO GENÉTICA
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ABNT
ZECHI-CEIDE, Roseli Maria et al. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf. Acesso em: 19 abr. 2024.
APA
Zechi-Ceide, R. M., Guion-Almeida, M. L., Oliveira, N. A. J., Richieri-Costa, A., & Passos-Bueno, M. R. (2009). Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf
NLM
Zechi-Ceide RM, Guion-Almeida ML, Oliveira NAJ, Richieri-Costa A, Passos-Bueno MR. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations [Internet]. Anais. 2009 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf
Vancouver
Zechi-Ceide RM, Guion-Almeida ML, Oliveira NAJ, Richieri-Costa A, Passos-Bueno MR. Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations [Internet]. Anais. 2009 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/ba673f31-b648-4c20-a481-a147f49859c6/3100222.pdf
Artigo de periodico
Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients (1992)
Nardi, Aguinaldo César ; Ferreira, Ubirajara; Rodrigues Netto, Nelson; Magna, Luís Alberto; Rodini, Elaine Sbroggio de Oliveira; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: SISTEMA URINARIO (FISIOLOGIA)
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ABNT
NARDI, Aguinaldo César et al. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics, v. 44, n. 6, p. 803-806, 1992Tradução . . Acesso em: 19 abr. 2024.
APA
Nardi, A. C., Ferreira, U., Rodrigues Netto, N., Magna, L. A., Rodini, E. S. de O., & Richieri-Costa, A. (1992). Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics, 44( 6), 803-806.
NLM
Nardi AC, Ferreira U, Rodrigues Netto N, Magna LA, Rodini ES de O, Richieri-Costa A. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics. 1992 ; 44( 6): 803-806.[citado 2024 abr. 19 ]
Vancouver
Nardi AC, Ferreira U, Rodrigues Netto N, Magna LA, Rodini ES de O, Richieri-Costa A. Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients. American Journal of Medical Genetics. 1992 ; 44( 6): 803-806.[citado 2024 abr. 19 ]
Artigo de periodico
Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene (2008)
Ceide, Roseli Maria Zechi; Oliveira, Nélio Alessandro de Jesus; Guion-Almeida, Maria Leine; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita
Source: Clinical Dysmorphology. Unidades: HRAC, IB
Subjects: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENES
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ABNT
CEIDE, Roseli Maria Zechi et al. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, v. 17, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3282fe1b8e. Acesso em: 19 abr. 2024.
APA
Ceide, R. M. Z., Oliveira, N. A. de J., Guion-Almeida, M. L., Antunes, L. F. B. B., Richieri-Costa, A., & Passos-Bueno, M. R. (2008). Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, 17( 3), 225-226. doi:10.1097/mcd.0b013e3282fe1b8e
NLM
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Vancouver
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Trabalho de evento-resumo
Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 (2019)
Nakata, Nancy Mizue Kokitsu ; Jehee, F; Sandri, R; Pittoli, Siulan Vendramini Paulovich ; Alvarez, Camila Wenceslau ; Monteiro, R; Mazzeu, J; Zechi-Ceide, Roseli Maria ; Richieri-Costa, Antonio
Source: Utrecht: European Cleft Palate Craniofacial Association, 2019. Conference titles: European Cleft Palate Craniofacial Association Congress. Unidade: HRAC
Subjects: FENÓTIPOS, SÍNDROME DE PIERRE ROBIN, DELEÇÃO DE GENES
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ABNT
NAKATA, Nancy Mizue Kokitsu et al. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3. 2019, Anais.. Utrecht: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf. Acesso em: 19 abr. 2024.
APA
Nakata, N. M. K., Jehee, F., Sandri, R., Pittoli, S. V. P., Alvarez, C. W., Monteiro, R., et al. (2019). Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3. In Utrecht: European Cleft Palate Craniofacial Association, 2019. Utrecht: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
NLM
Nakata NMK, Jehee F, Sandri R, Pittoli SVP, Alvarez CW, Monteiro R, Mazzeu J, Zechi-Ceide RM, Richieri-Costa A. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 [Internet]. Utrecht: European Cleft Palate Craniofacial Association, 2019. 2019 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
Vancouver
Nakata NMK, Jehee F, Sandri R, Pittoli SVP, Alvarez CW, Monteiro R, Mazzeu J, Zechi-Ceide RM, Richieri-Costa A. Unique phenotype in a Brazilian girl with syndromic Robin sequence and a 5.6 mb deletion in xp11.4p11.3 [Internet]. Utrecht: European Cleft Palate Craniofacial Association, 2019. 2019 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/2f17e911-522c-4ebf-b07d-80b7f922a17c/2963227.pdf
Artigo de periodico
Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly (2012)
Roessler, E; Hu, Ping; Hong, Sung-Kook; Srivastava, Kshitij; Carrington, Blake; Sood, Raman; Petrykowska, Hanna; Elnitski, Laura; Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio ; Feldman, Benjamin; Odenwald, Ward F.; Muenke, Maximilian
Source: PLOS ONE. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, GENÉTICA
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ABNT
ROESSLER, E et al. Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly. PLOS ONE, v. 7, n. 7, p. e39026, 2012Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0039026. Acesso em: 19 abr. 2024.
APA
Roessler, E., Hu, P., Hong, S. -K., Srivastava, K., Carrington, B., Sood, R., et al. (2012). Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly. PLOS ONE, 7( 7), e39026. doi:10.1371/journal.pone.0039026
NLM
Roessler E, Hu P, Hong S-K, Srivastava K, Carrington B, Sood R, Petrykowska H, Elnitski L, Ribeiro LA, Richieri-Costa A, Feldman B, Odenwald WF, Muenke M. Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly [Internet]. PLOS ONE. 2012 ; 7( 7): e39026.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1371/journal.pone.0039026
Vancouver
Roessler E, Hu P, Hong S-K, Srivastava K, Carrington B, Sood R, Petrykowska H, Elnitski L, Ribeiro LA, Richieri-Costa A, Feldman B, Odenwald WF, Muenke M. Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly [Internet]. PLOS ONE. 2012 ; 7( 7): e39026.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1371/journal.pone.0039026
Artigo de periodico
Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families (1986)
Richieri-Costa, Antonio; Opitz, John M.
Source: American Journal of Medical Genetics Supplement. Unidade: HRAC
Subjects: HETEROGENEIDADE, ANORMALIDADES CONGÊNITAS
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ABNT
RICHIERI-COSTA, Antonio e OPITZ, John M. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families. American Journal of Medical Genetics Supplement, v. 24, p. 195-206, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320250624. Acesso em: 19 abr. 2024.
APA
Richieri-Costa, A., & Opitz, J. M. (1986). Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families. American Journal of Medical Genetics Supplement, 24, 195-206. doi:10.1002/ajmg.1320250624
NLM
Richieri-Costa A, Opitz JM. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families [Internet]. American Journal of Medical Genetics Supplement. 1986 ; 24 195-206.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320250624
Vancouver
Richieri-Costa A, Opitz JM. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families [Internet]. American Journal of Medical Genetics Supplement. 1986 ; 24 195-206.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.1320250624
Artigo de periodico
Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 (2007)
Sandrin-Garcia, Paula; Abramides, Dagma Venturini Marques; Martelli, Lúcia Regina; Ramos, Ester Silveira; Richieri-Costa, Antonio; Passos, Geraldo Aleixo Silva
Source: Molecular and Cellular Biochemistry. Unidades: FOB, FMRP, HRAC, FORP
Subjects: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN-GARCIA, Paula et al. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, v. 303, n. 1/2, p. 9-17, 2007Tradução . . Disponível em: https://doi.org/10.1007/s11010-007-9450-5. Acesso em: 19 abr. 2024.
APA
Sandrin-Garcia, P., Abramides, D. V. M., Martelli, L. R., Ramos, E. S., Richieri-Costa, A., & Passos, G. A. S. (2007). Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, 303( 1/2), 9-17. doi:10.1007/s11010-007-9450-5
NLM
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Vancouver
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Artigo de periodico
Turner syndrome in diverse populations (2020)
Kruszka, Paul ; Addissie, Yonit A; Tekendo-Ngongang, Cedrik; Jones, Kelly L ; Savage, Sarah K.; Gupta, Neerja; Sirisena, Nirmala D; Dissanayake, Vajira H. W; Paththinige, C. Sampath; Aravena, Teresa; Nampoothiri, Sheela; Yesodharan, Dhanya; Girisha, Katta M ; Patil, Siddaramappa Jagdish ; Jamuar, Saumya Shekhar ; Goh, Jasmine Chew-Yin; Utari, Agustini ; Sihombing, Nydia; Mishra, Rupesh; Chitrakar, Neer Shoba; Iriele, Brenda C.; Lulseged, Ezana; Megarbane, Andre ; Uwineza, Annette; Oyenusi, Elizabeth Eberechi; Olopade, Oluwarotimi Bolaji; Fasanmade, Olufemi Adetola; Duenas-Roque, Milagros M.; Thong, Meow-Keong; Tung, Joanna Y. L; Mok, Gary T. K; Fleischer, Nicole; Rwegerera, Godfrey M; Herreros, María Beatriz; Watts, Johnathan; Fieggen, Karen; Huckstadt, Victoria; Moresco, Angélica; Obregon, María Gabriela; Hussen, Dalia Farouk; Ashaat, Neveen A ; Ashaat, Engy A. ; Chung, Brian H. Y; Badoe, Eben; Faradz, Sultana M. H; El Ruby, Mona O; Shotelersuk, Vorasuk; Wonkam, Ambroise; Ekure, Ekanem Nsikak; Phadke, Shubha R; Richieri-Costa, Antonio ; Muenke, Maximilian
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANÁLISE FACIAL, GENÉTICA DE POPULAÇÕES, FENÓTIPOS, ANORMALIDADES CONGÊNITAS, SÍNDROME DE NOONAN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KRUSZKA, Paul et al. Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 182A, n. 2, p. 303-313, 2020Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61461. Acesso em: 19 abr. 2024.
APA
Kruszka, P., Addissie, Y. A., Tekendo-Ngongang, C., Jones, K. L., Savage, S. K., Gupta, N., et al. (2020). Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, 182A( 2), 303-313. doi:10.1002/ajmg.a.61461
NLM
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.61461
Vancouver
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.61461
Trabalho de evento-resumo
Triopia associated with a large facial cleft: report on a brazilian patient (2001)
Moretti Ferreira, Danilo ; Lima, Renata Lúcia Leite Ferreira de; Murray, Jeffrey C; Richieri-Costa, Antonio
Source: Programme & Abstracts. Conference titles: International Congress on Cleft Palate and Related Craniofacial Anomalies. Unidade: HRAC
Assunto: ANOMALIA CRANIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORETTI FERREIRA, Danilo et al. Triopia associated with a large facial cleft: report on a brazilian patient. 2001, Anais.. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2001. Disponível em: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf. Acesso em: 19 abr. 2024.
APA
Moretti Ferreira, D., Lima, R. L. L. F. de, Murray, J. C., & Richieri-Costa, A. (2001). Triopia associated with a large facial cleft: report on a brazilian patient. In Programme & Abstracts. Goteborg: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf
NLM
Moretti Ferreira D, Lima RLLF de, Murray JC, Richieri-Costa A. Triopia associated with a large facial cleft: report on a brazilian patient [Internet]. Programme & Abstracts. 2001 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf
Vancouver
Moretti Ferreira D, Lima RLLF de, Murray JC, Richieri-Costa A. Triopia associated with a large facial cleft: report on a brazilian patient [Internet]. Programme & Abstracts. 2001 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/11fb802c-7472-4676-9bc0-854a0a1820fe/3167153.pdf
Artigo de periodico
Trigonocephaly (1992)
Zanini, S A; Paglioli Neto, E; Viterbo, F; Richieri-Costa, A; Tershakowec, M
Source: Journal of Craniofacial Surgery. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANINI, S A et al. Trigonocephaly. Journal of Craniofacial Surgery, v. 3 , n. 2 , p. se 1992, 1992Tradução . . Disponível em: https://doi.org/10.1097/00006534-198508000-00005. Acesso em: 19 abr. 2024.
APA
Zanini, S. A., Paglioli Neto, E., Viterbo, F., Richieri-Costa, A., & Tershakowec, M. (1992). Trigonocephaly. Journal of Craniofacial Surgery, 3 ( 2 ), se 1992. doi:10.1097/00006534-198508000-00005
NLM
Zanini SA, Paglioli Neto E, Viterbo F, Richieri-Costa A, Tershakowec M. Trigonocephaly [Internet]. Journal of Craniofacial Surgery. 1992 ;3 ( 2 ): se 1992.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00006534-198508000-00005
Vancouver
Zanini SA, Paglioli Neto E, Viterbo F, Richieri-Costa A, Tershakowec M. Trigonocephaly [Internet]. Journal of Craniofacial Surgery. 1992 ;3 ( 2 ): se 1992.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00006534-198508000-00005
Artigo de periodico
Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study (2004)
Passos-Bueno, Maria Rita ; Gaspar, Dinamar A.; Kamiya, Tânia Yoshico; Tescarollo, Graziela; Rabanéa, Daniel Saraiva; Richieri-Costa, Antonio; Alonso, Nivaldo; Araújo, Belmino
Source: The Cleft Palate-Craniofacial Journal. Unidades: IB, HRAC
Subjects: GENES, FISSURA LÁBIOPALATINA, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, v. 41, n. 4, p. 387-391, 2004Tradução . . Acesso em: 19 abr. 2024.
APA
Passos-Bueno, M. R., Gaspar, D. A., Kamiya, T. Y., Tescarollo, G., Rabanéa, D. S., Richieri-Costa, A., et al. (2004). Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, 41( 4), 387-391.
NLM
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 abr. 19 ]
Vancouver
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 abr. 19 ]
Trabalho de evento-resumo
Tooth abnormalities in the Richieri-Costa-Pereira syndrome (2013)
Passos, Vivian Agostino Biella; Severini, Janete Mary Baaclini Galante; Dalben, Gisele da Silva; Richieri-Costa, Antonio; Ozawa, Terumi Okada
Source: Anais. Conference titles: International Congress on Cleft Lip/Palate and Related Craniofacial Anomalies. Unidade: HRAC
Subjects: ANOMALIA DENTÁRIA, DISOSTOSE MANDIBULOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS, Vivian Agostino Biella et al. Tooth abnormalities in the Richieri-Costa-Pereira syndrome. 2013, Anais.. Orlando: American Cleft Palate-Craniofacial Association (ACPA), 2013. . Acesso em: 19 abr. 2024.
APA
Passos, V. A. B., Severini, J. M. B. G., Dalben, G. da S., Richieri-Costa, A., & Ozawa, T. O. (2013). Tooth abnormalities in the Richieri-Costa-Pereira syndrome. In Anais. Orlando: American Cleft Palate-Craniofacial Association (ACPA).
NLM
Passos VAB, Severini JMBG, Dalben G da S, Richieri-Costa A, Ozawa TO. Tooth abnormalities in the Richieri-Costa-Pereira syndrome. Anais. 2013 ;[citado 2024 abr. 19 ]
Vancouver
Passos VAB, Severini JMBG, Dalben G da S, Richieri-Costa A, Ozawa TO. Tooth abnormalities in the Richieri-Costa-Pereira syndrome. Anais. 2013 ;[citado 2024 abr. 19 ]
Trabalho de evento-resumo
Tooth abnormalities in individuals with velocardiofacial syndrome (2013)
Santos, J. B.; Dalben, Gisele da Silva ; Taveira, Luís Antônio de Assis; Richieri-Costa, Antonio ; Neves, Lucimara Teixeira das
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRAC, FOB
Subjects: ANOMALIA DENTÁRIA, PREVALÊNCIA, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, J. B. et al. Tooth abnormalities in individuals with velocardiofacial syndrome. 2013, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013. Disponível em: https://repositorio.usp.br/directbitstream/3cced6db-b830-4774-ae69-697de7b8a793/2513380.pdf. Acesso em: 19 abr. 2024.
APA
Santos, J. B., Dalben, G. da S., Taveira, L. A. de A., Richieri-Costa, A., & Neves, L. T. das. (2013). Tooth abnormalities in individuals with velocardiofacial syndrome. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/3cced6db-b830-4774-ae69-697de7b8a793/2513380.pdf
NLM
Santos JB, Dalben G da S, Taveira LA de A, Richieri-Costa A, Neves LT das. Tooth abnormalities in individuals with velocardiofacial syndrome [Internet]. Anais. 2013 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/3cced6db-b830-4774-ae69-697de7b8a793/2513380.pdf
Vancouver
Santos JB, Dalben G da S, Taveira LA de A, Richieri-Costa A, Neves LT das. Tooth abnormalities in individuals with velocardiofacial syndrome [Internet]. Anais. 2013 ;[citado 2024 abr. 19 ] Available from: https://repositorio.usp.br/directbitstream/3cced6db-b830-4774-ae69-697de7b8a793/2513380.pdf
Artigo de periodico
Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome (2008)
Dalben, Gisele da Silva; Richieri-Costa, Antonio; Taveira, Lúis Antonio de Assis
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. Unidades: HRAC, FOB
Subjects: DENTE SUPRANUMERÁRIO, DENTE (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva e RICHIERI-COSTA, Antonio e TAVEIRA, Lúis Antonio de Assis. Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, v. 106, p. e46-e51, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tripleo.2008.04.019. Acesso em: 19 abr. 2024.
APA
Dalben, G. da S., Richieri-Costa, A., & Taveira, L. A. de A. (2008). Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 106, e46-e51. doi:10.1016/j.tripleo.2008.04.019
NLM
Dalben G da S, Richieri-Costa A, Taveira LA de A. Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome [Internet]. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 2008 ; 106 e46-e51.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.tripleo.2008.04.019
Vancouver
Dalben G da S, Richieri-Costa A, Taveira LA de A. Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome [Internet]. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 2008 ; 106 e46-e51.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.tripleo.2008.04.019

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