Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome? (1989)
- Authors:
- USP affiliated authors: ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.1320330406
- Subjects: ANORMALIDADES MÚLTIPLAS; DISOSTOSE MANDIBULOFACIAL; GRAVIDEZ NO DIABETES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 33, n. 4, p. 450-452, Aug. 1989
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine. Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome?. American Journal of Medical Genetics, v. 33, n. 4, p. 450-452, 1989Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320330406. Acesso em: 20 abr. 2024. -
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1989). Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome? American Journal of Medical Genetics, 33( 4), 450-452. doi:10.1002/ajmg.1320330406 -
NLM
Richieri-Costa A, Guion-Almeida ML. Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome? [Internet]. American Journal of Medical Genetics. 1989 ; 33( 4): 450-452.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1002/ajmg.1320330406 -
Vancouver
Richieri-Costa A, Guion-Almeida ML. Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome? [Internet]. American Journal of Medical Genetics. 1989 ; 33( 4): 450-452.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1002/ajmg.1320330406 - Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study
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- 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
Informações sobre o DOI: 10.1002/ajmg.1320330406 (Fonte: oaDOI API)
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