Ohdo syndrome: report on a brazilian girl with additional findings (1997)
- Authors:
- Autor USP: ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- DOI: 10.1111/j.1399-0004.1997.tb02468.x
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Genetics
- Volume/Número/Paginação/Ano: v.51, n.4, p.268-270, Apr. 1997
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
LOPES, Vera Lúcia Gil da Silva e GUION-ALMEIDA, Maria Leine. Ohdo syndrome: report on a brazilian girl with additional findings. Clinical Genetics, v. 51, n. 4, p. 268-270, 1997Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.1997.tb02468.x. Acesso em: 19 out. 2024. -
APA
Lopes, V. L. G. da S., & Guion-Almeida, M. L. (1997). Ohdo syndrome: report on a brazilian girl with additional findings. Clinical Genetics, 51( 4), 268-270. doi:10.1111/j.1399-0004.1997.tb02468.x -
NLM
Lopes VLG da S, Guion-Almeida ML. Ohdo syndrome: report on a brazilian girl with additional findings [Internet]. Clinical Genetics. 1997 ;51( 4): 268-270.[citado 2024 out. 19 ] Available from: https://doi.org/10.1111/j.1399-0004.1997.tb02468.x -
Vancouver
Lopes VLG da S, Guion-Almeida ML. Ohdo syndrome: report on a brazilian girl with additional findings [Internet]. Clinical Genetics. 1997 ;51( 4): 268-270.[citado 2024 out. 19 ] Available from: https://doi.org/10.1111/j.1399-0004.1997.tb02468.x - 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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Informações sobre o DOI: 10.1111/j.1399-0004.1997.tb02468.x (Fonte: oaDOI API)
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