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Artigo de periodico
A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate (2006)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Tabith Junior, Alfredo
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, v. 15, n. 3, p. 171-174, 2006Tradução . . Disponível em: https://doi.org/10.1097/01.mcd.0000220603.09661.7e. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Tabith Junior, A. (2006). A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, 15( 3), 171-174. doi:10.1097/01.mcd.0000220603.09661.7e
NLM
Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e
Vancouver
Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e
Artigo de periodico
A importância das próteses provisórias (2003)
Neppelenbroek, Karin Hermana; Lopes, José Fernando Scarelli; Silva, Regina Helena B. T.; Segalla, José Cláudio Martins
Source: Revista Gaúcha de Odontologia. Unidade: HRAC
Subjects: PRÓTESE PARCIAL FIXA, COROAS DENTÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NEPPELENBROEK, Karin Hermana et al. A importância das próteses provisórias. Revista Gaúcha de Odontologia, v. 51, n. ja/mar., p. 50-53, 2003Tradução . . Acesso em: 19 abr. 2024.
APA
Neppelenbroek, K. H., Lopes, J. F. S., Silva, R. H. B. T., & Segalla, J. C. M. (2003). A importância das próteses provisórias. Revista Gaúcha de Odontologia, 51( ja/mar.), 50-53.
NLM
Neppelenbroek KH, Lopes JFS, Silva RHBT, Segalla JCM. A importância das próteses provisórias. Revista Gaúcha de Odontologia. 2003 ; 51( ja/mar.): 50-53.[citado 2024 abr. 19 ]
Vancouver
Neppelenbroek KH, Lopes JFS, Silva RHBT, Segalla JCM. A importância das próteses provisórias. Revista Gaúcha de Odontologia. 2003 ; 51( ja/mar.): 50-53.[citado 2024 abr. 19 ]
Artigo de periodico
Intentional ankylosis of deciduous canines to reinforce maxillary protraction (2003)
Silva Filho, Omar Gabriel da; Ozawa, Terumi Okada; Okada, Celeste Hiromi; Okada, Helena Yuko; Carvalho, Roberta Martinelli
Source: Journal of Clinical Orthodontics. Unidade: HRAC
Subjects: ANQUILOSE, DENTE DECÍDUO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Intentional ankylosis of deciduous canines to reinforce maxillary protraction. Journal of Clinical Orthodontics, v. 37, n. 6, p. 315-320, 2003Tradução . . Acesso em: 19 abr. 2024.
APA
Silva Filho, O. G. da, Ozawa, T. O., Okada, C. H., Okada, H. Y., & Carvalho, R. M. (2003). Intentional ankylosis of deciduous canines to reinforce maxillary protraction. Journal of Clinical Orthodontics, 37( 6), 315-320.
NLM
Silva Filho OG da, Ozawa TO, Okada CH, Okada HY, Carvalho RM. Intentional ankylosis of deciduous canines to reinforce maxillary protraction. Journal of Clinical Orthodontics. 2003 ; 37( 6): 315-320.[citado 2024 abr. 19 ]
Vancouver
Silva Filho OG da, Ozawa TO, Okada CH, Okada HY, Carvalho RM. Intentional ankylosis of deciduous canines to reinforce maxillary protraction. Journal of Clinical Orthodontics. 2003 ; 37( 6): 315-320.[citado 2024 abr. 19 ]
Artigo de periodico
Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype (2001)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: RETARDO MENTAL, GENÉTICA MÉDICA
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 dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype. Clinical Dysmorphology, v. 10, n. 2, p. 81-86, 2001Tradução . . Disponível em: https://doi.org/10.1097/00019605-200104000-00002. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2001). Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype. Clinical Dysmorphology, 10( 2), 81-86. doi:10.1097/00019605-200104000-00002
NLM
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype [Internet]. Clinical Dysmorphology. 2001 ; 10( 2): 81-86.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-200104000-00002
Vancouver
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation and CNS structural anomalies: defining the phenotype [Internet]. Clinical Dysmorphology. 2001 ; 10( 2): 81-86.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-200104000-00002
Artigo de periodico
Secondary bone graft and eruption of the permanent canine in patients with alveolar clefts: literature review and case report (2000)
Silva Filho, Omar Gabriel da; Teles, Silvana Ghilardi; Ozawa, Terumi Okada; Capelozza Filho, Leopoldino
Source: Angle Orthodontist. Unidades: HRAC, FOB
Subjects: ODONTOPEDIATRIA, LÁBIO FISSURADO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Secondary bone graft and eruption of the permanent canine in patients with alveolar clefts: literature review and case report. Angle Orthodontist, v. 70, n. 2, p. 174-178, 2000Tradução . . Acesso em: 19 abr. 2024.
APA
Silva Filho, O. G. da, Teles, S. G., Ozawa, T. O., & Capelozza Filho, L. (2000). Secondary bone graft and eruption of the permanent canine in patients with alveolar clefts: literature review and case report. Angle Orthodontist, 70( 2), 174-178.
NLM
Silva Filho OG da, Teles SG, Ozawa TO, Capelozza Filho L. Secondary bone graft and eruption of the permanent canine in patients with alveolar clefts: literature review and case report. Angle Orthodontist. 2000 ; 70( 2): 174-178.[citado 2024 abr. 19 ]
Vancouver
Silva Filho OG da, Teles SG, Ozawa TO, Capelozza Filho L. Secondary bone graft and eruption of the permanent canine in patients with alveolar clefts: literature review and case report. Angle Orthodontist. 2000 ; 70( 2): 174-178.[citado 2024 abr. 19 ]
Artigo de periodico
Prevalence of intranasal ectopic teeth in children with complete unilateral and bilateral cleft lip and palate (2000)
Medeiros, Alexandra Sárzyla; Gomide, Márcia Ribeiro; Costa, Beatriz; Carrara, Cleide Felicio de Carvalho; Neves, Lucimara Teixeira das
Source: The Cleft Palate-Craniofacial Journal. Unidade: HRAC
Subjects: ODONTOPEDIATRIA, LÁBIO FISSURADO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS, Alexandra Sárzyla et al. Prevalence of intranasal ectopic teeth in children with complete unilateral and bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 37, n. 3, p. 271-273, 2000Tradução . . Acesso em: 19 abr. 2024.
APA
Medeiros, A. S., Gomide, M. R., Costa, B., Carrara, C. F. de C., & Neves, L. T. das. (2000). Prevalence of intranasal ectopic teeth in children with complete unilateral and bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, 37( 3), 271-273.
NLM
Medeiros AS, Gomide MR, Costa B, Carrara CF de C, Neves LT das. Prevalence of intranasal ectopic teeth in children with complete unilateral and bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2000 ; 37( 3): 271-273.[citado 2024 abr. 19 ]
Vancouver
Medeiros AS, Gomide MR, Costa B, Carrara CF de C, Neves LT das. Prevalence of intranasal ectopic teeth in children with complete unilateral and bilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal. 2000 ; 37( 3): 271-273.[citado 2024 abr. 19 ]
Artigo de periodico
Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome (2000)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology, v. 9, n. 4, p. 269-272, 2000Tradução . . Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (2000). Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology, 9( 4), 269-272.
NLM
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology. 2000 ; 9( 4): 269-272.[citado 2024 abr. 19 ]
Vancouver
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Cleft lip/palate abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome. Clinical Dysmorphology. 2000 ; 9( 4): 269-272.[citado 2024 abr. 19 ]
Artigo de periodico
Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome (2000)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome. Clinical Dysmorphology, v. 9, n. 4, p. 297-299, 2000Tradução . . Disponível em: https://doi.org/10.1097/00019605-200009040-00016. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2000). Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome. Clinical Dysmorphology, 9( 4), 297-299. doi:10.1097/00019605-200009040-00016
NLM
Guion-Almeida ML, Richieri-Costa A. Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome [Internet]. Clinical Dysmorphology. 2000 ; 9( 4): 297-299.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-200009040-00016
Vancouver
Guion-Almeida ML, Richieri-Costa A. Amniotic band sequence versus the autosomal recessive microcephaly, facial clefting, and preaxial polydactyly syndrome [Internet]. Clinical Dysmorphology. 2000 ; 9( 4): 297-299.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-200009040-00016
Artigo de periodico
Correction of posterior crossbite in the primary dentition (2000)
Silva Filho, Omar Gabriel da; Ferrari Junior, Flávio Mauro; Aiello, Carlos Alberto; Zopone, Nárima
Source: Journal of Clinical Pediatric Dentistry. Unidade: HRAC
Assunto: ODONTOPEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA FILHO, Omar Gabriel da et al. Correction of posterior crossbite in the primary dentition. Journal of Clinical Pediatric Dentistry, v. 24, n. 3, p. 165-180, 2000Tradução . . Acesso em: 19 abr. 2024.
APA
Silva Filho, O. G. da, Ferrari Junior, F. M., Aiello, C. A., & Zopone, N. (2000). Correction of posterior crossbite in the primary dentition. Journal of Clinical Pediatric Dentistry, 24( 3), 165-180.
NLM
Silva Filho OG da, Ferrari Junior FM, Aiello CA, Zopone N. Correction of posterior crossbite in the primary dentition. Journal of Clinical Pediatric Dentistry. 2000 ; 24( 3): 165-180.[citado 2024 abr. 19 ]
Vancouver
Silva Filho OG da, Ferrari Junior FM, Aiello CA, Zopone N. Correction of posterior crossbite in the primary dentition. Journal of Clinical Pediatric Dentistry. 2000 ; 24( 3): 165-180.[citado 2024 abr. 19 ]
Artigo de periodico
Dental anesthetic procedures for cleft lip and palate patients (2000)
Dalben, Gisele da Silva; Costa, Beatriz; Gomide, Márcia Ribeiro; Neves, Lucimara Teixeira das
Source: Journal of Clinical Pediatric Dentistry. Unidade: HRAC
Subjects: ANESTESIA ODONTOLÓGICA, LÁBIO FISSURADO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva et al. Dental anesthetic procedures for cleft lip and palate patients. Journal of Clinical Pediatric Dentistry, v. 24, n. 3, p. 153-158, 2000Tradução . . Acesso em: 19 abr. 2024.
APA
Dalben, G. da S., Costa, B., Gomide, M. R., & Neves, L. T. das. (2000). Dental anesthetic procedures for cleft lip and palate patients. Journal of Clinical Pediatric Dentistry, 24( 3), 153-158.
NLM
Dalben G da S, Costa B, Gomide MR, Neves LT das. Dental anesthetic procedures for cleft lip and palate patients. Journal of Clinical Pediatric Dentistry. 2000 ; 24( 3): 153-158.[citado 2024 abr. 19 ]
Vancouver
Dalben G da S, Costa B, Gomide MR, Neves LT das. Dental anesthetic procedures for cleft lip and palate patients. Journal of Clinical Pediatric Dentistry. 2000 ; 24( 3): 153-158.[citado 2024 abr. 19 ]
Artigo de periodico
"New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family (2000)
Zanchetta, Sthella; Ohara, Kouzaburo; Rodrigues, Patrícia T.; Carvalho, Ester L. L.; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANCHETTA, Sthella et al. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, v. No 2000, n. 1, p. 13-16, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t. Acesso em: 19 abr. 2024.
APA
Zanchetta, S., Ohara, K., Rodrigues, P. T., Carvalho, E. L. L., & Richieri-Costa, A. (2000). "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, No 2000( 1), 13-16. doi:10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
NLM
Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family [Internet]. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
Vancouver
Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family [Internet]. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
Artigo de periodico
Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients (1999)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 1, p. 72-77, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, No 1999( 1), 72-77. doi:10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
NLM
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
Vancouver
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
Artigo de periodico
Mandibulofacial dysostosis Bauru type syndrome: a new case (1999)
Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, v. 86, n. 2, p. 199-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g. Acesso em: 19 abr. 2024.
APA
Ceide, R. M. Z., & Guion-Almeida, M. L. (1999). Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, 86( 2), 199-201. doi:10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
NLM
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
Vancouver
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
Artigo de periodico
Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: a new syndrome? (1999)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Clinical Dysmophology. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
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 dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: a new syndrome?. Clinical Dysmophology, v. 8, n. 1, p. 1-4, 1999Tradução . . Disponível em: https://doi.org/10.1097/00019605-199901000-00001. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1999). Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: a new syndrome? Clinical Dysmophology, 8( 1), 1-4. doi:10.1097/00019605-199901000-00001
NLM
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: a new syndrome? [Internet]. Clinical Dysmophology. 1999 ; 8( 1): 1-4.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-199901000-00001
Vancouver
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies: a new syndrome? [Internet]. Clinical Dysmophology. 1999 ; 8( 1): 1-4.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1097/00019605-199901000-00001
Artigo de periodico
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
Wallis, Deeann E.; Roessler, Erich; Hehr, Ute; Nanni, Luisa; Wiltshire, Tim; Richieri-Costa, Antonio; Gillessen-Kaesbach, Gabriele; Zackai, Elaine H.; Rommens, Johanna; Muenke, Maximilian
Source: Nature Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WALLIS, Deeann E. et al. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, v. 22, n. 2, p. 196-198, 1999Tradução . . Disponível em: https://doi.org/10.1038/9718. Acesso em: 19 abr. 2024.
APA
Wallis, D. E., Roessler, E., Hehr, U., Nanni, L., Wiltshire, T., Richieri-Costa, A., et al. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, 22( 2), 196-198. doi:10.1038/9718
NLM
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1038/9718
Vancouver
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1038/9718
Artigo de periodico
Lower lip pits and anorectal anomalies in Kabuki syndrome (1999)
Nakata, Nancy Mizue Kokitsu; Vendramini, Siulan; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu e VENDRAMINI, Siulan e GUION-ALMEIDA, Maria Leine. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, v. 86, n. 3, p. 282-284, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h. Acesso em: 19 abr. 2024.
APA
Nakata, N. M. K., Vendramini, S., & Guion-Almeida, M. L. (1999). Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, 86( 3), 282-284. doi:10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
NLM
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
Vancouver
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
Artigo de periodico
New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients (1999)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 3, p. 237-244, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1999). New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, No 1999( 3), 237-244. doi:10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i
NLM
Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i
Vancouver
Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i

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