ReP USP - Resultado da busca

Artigo de periodico
Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies (2012)
Ribeiro-Bicudo, Lucilene Arilho ; Quiezi, Rodrigo Gonçalves; Guion-Almeida, Maria Leine; Legnaro, Chiara; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, SÍNDROMES OROFACIODIGITAIS
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ABNT
RIBEIRO-BICUDO, Lucilene Arilho et al. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, v. 158A, n. 5, p. 1233-1235, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35305. Acesso em: 27 abr. 2024.
APA
Ribeiro-Bicudo, L. A., Quiezi, R. G., Guion-Almeida, M. L., Legnaro, C., & Richieri-Costa, A. (2012). Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, 158A( 5), 1233-1235. doi:10.1002/ajmg.a.35305
NLM
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.35305
Vancouver
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.35305
Artigo de periodico
Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: a new subtype of frontonasal dysgenesis (2010)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Assunto: ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: a new subtype of frontonasal dysgenesis. American Journal of Medical Genetics, Part A, v. 152A, n. 8, p. 2039-2042, 2010Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33485. Acesso em: 27 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2010). Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: a new subtype of frontonasal dysgenesis. American Journal of Medical Genetics, Part A, 152A( 8), 2039-2042. doi:10.1002/ajmg.a.33485
NLM
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: a new subtype of frontonasal dysgenesis [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 8): 2039-2042.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33485
Vancouver
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: a new subtype of frontonasal dysgenesis [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 8): 2039-2042.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33485
Artigo de periodico
Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: a new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome? (2010)
Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine; Jehee, Fernanda Sarquis; Rocha, Kátia Maria da; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics, Part A. Unidades: HRAC, IB
Subjects: DISOSTOSE MANDIBULOFACIAL, PÁLPEBRAS (ANORMALIDADES), FISSURA PALATINA, ALOPECIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi et al. Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: a new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome?. American Journal of Medical Genetics, Part A, v. 152A, n. 7, p. 1838-1840, 2010Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33477. Acesso em: 27 abr. 2024.
APA
Ceide, R. M. Z., Guion-Almeida, M. L., Jehee, F. S., Rocha, K. M. da, & Passos-Bueno, M. R. (2010). Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: a new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome? American Journal of Medical Genetics, Part A, 152A( 7), 1838-1840. doi:10.1002/ajmg.a.33477
NLM
Ceide RMZ, Guion-Almeida ML, Jehee FS, Rocha KM da, Passos-Bueno MR. Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: a new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome? [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 7): 1838-1840.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33477
Vancouver
Ceide RMZ, Guion-Almeida ML, Jehee FS, Rocha KM da, Passos-Bueno MR. Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: a new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome? [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 7): 1838-1840.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33477
Artigo de periodico
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: report of four brazilian patients (2010)
Ribeiro, Lucilene Arilho; Quiezi, Rodrigo Gonçalves; Nascimento, Adriana; Bertolacini, Claudia Danielli Pereira; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, RESSONÂNCIA MAGNÉTICA, SEQUENCIAMENTO GENÉTICO, EDUCAÇÃO INFANTIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho et al. Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: report of four brazilian patients. American Journal of Medical Genetics, Part A, v. 152A, n. 7, p. 1688-1694, 2010Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33466. Acesso em: 27 abr. 2024.
APA
Ribeiro, L. A., Quiezi, R. G., Nascimento, A., Bertolacini, C. D. P., & Richieri-Costa, A. (2010). Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: report of four brazilian patients. American Journal of Medical Genetics, Part A, 152A( 7), 1688-1694. doi:10.1002/ajmg.a.33466
NLM
Ribeiro LA, Quiezi RG, Nascimento A, Bertolacini CDP, Richieri-Costa A. Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: report of four brazilian patients [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 7): 1688-1694.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33466
Vancouver
Ribeiro LA, Quiezi RG, Nascimento A, Bertolacini CDP, Richieri-Costa A. Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: report of four brazilian patients [Internet]. American Journal of Medical Genetics, Part A. 2010 ; 152A( 7): 1688-1694.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.33466
Artigo de periodico
Nonsyndromic alar clefts: report of five brazilian patients (2009)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Subjects: ANOMALIA CRANIOFACIAL, NARIZ (ANATOMIA) (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine. Nonsyndromic alar clefts: report of five brazilian patients. American Journal of Medical Genetics, Part A, v. 149A, n. 12, p. 2765-2767, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32845. Acesso em: 27 abr. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (2009). Nonsyndromic alar clefts: report of five brazilian patients. American Journal of Medical Genetics, Part A, 149A( 12), 2765-2767. doi:10.1002/ajmg.a.32845
NLM
Richieri-Costa A, Guion-Almeida ML. Nonsyndromic alar clefts: report of five brazilian patients [Internet]. American Journal of Medical Genetics, Part A. 2009 ; 149A( 12): 2765-2767.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.32845
Vancouver
Richieri-Costa A, Guion-Almeida ML. Nonsyndromic alar clefts: report of five brazilian patients [Internet]. American Journal of Medical Genetics, Part A. 2009 ; 149A( 12): 2765-2767.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.32845
Artigo de periodico
Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype (2009)
Nakata, Nancy Mizue Kokitsu; Pittoli, Siulan Vendramini Pailovich; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Subjects: ANOMALIA CRANIOFACIAL, CÉREBRO (ANOMALIAS), SISTEMA NERVOSO CENTRAL (ANOMALIAS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu e PITTOLI, Siulan Vendramini Pailovich e RICHIERI-COSTA, Antonio. Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype. American Journal of Medical Genetics, Part A, v. 149A, n. 3, p. 519-520, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32588. Acesso em: 27 abr. 2024.
APA
Nakata, N. M. K., Pittoli, S. V. P., & Richieri-Costa, A. (2009). Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype. American Journal of Medical Genetics, Part A, 149A( 3), 519-520. doi:10.1002/ajmg.a.32588
NLM
Nakata NMK, Pittoli SVP, Richieri-Costa A. Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype [Internet]. American Journal of Medical Genetics, Part A. 2009 ; 149A( 3): 519-520.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.32588
Vancouver
Nakata NMK, Pittoli SVP, Richieri-Costa A. Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype [Internet]. American Journal of Medical Genetics, Part A. 2009 ; 149A( 3): 519-520.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.32588

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