Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents (1997)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e
- Subjects: ANORMALIDADES CRANIOFACIAIS; FISSURA LÁBIOPALATINA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 71, n. 2, p. 233-235, Aug. 1997
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, Antonio e BRANDÃO-ALMEIDA, Iara Lêda. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents. American Journal of Medical Genetics, v. 71, n. 2, p. 233-235, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e. Acesso em: 27 dez. 2025. -
APA
Richieri-Costa, A., & Brandão-Almeida, I. L. (1997). Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents. American Journal of Medical Genetics, 71( 2), 233-235. doi:10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e -
NLM
Richieri-Costa A, Brandão-Almeida IL. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 233-235.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e -
Vancouver
Richieri-Costa A, Brandão-Almeida IL. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected brazilian patient born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 233-235.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e - Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
- Tibial hemimelia: report of a new brazilian family an overview
- Atypical craniofacial clefts: a syndromological approach
- A década da linguagem: os genes começam a falar
- Estudo genético-clínico de 144 pacientes portadores de deficiência auditiva não sindrômica
- Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
- Perfil audiológico de indivíduos portadores da síndrome de Goldenhar
- Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
- Variable phenotypic manifestations of a K44N mutation in the TGIF gene
- PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
Informações sobre o DOI: 10.1002/(sici)1096-8628(19970808)71:2%3C233::aid-ajmg23%3E3.0.co;2-e (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas