Apparent malpuech syndrome: report on three Brazilian patients with additional signs (1995)
- Autor:
- Autor USP: ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.1320580104
- Assunto: GENÉTICA MÉDICA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 58, n. 1, p. 13-17, July 1995
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
GUION-ALMEIDA, Maria Leine. Apparent malpuech syndrome: report on three Brazilian patients with additional signs. American Journal of Medical Genetics, v. 58, n. 1, p. 13-17, 1995Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320580104. Acesso em: 23 abr. 2024. -
APA
Guion-Almeida, M. L. (1995). Apparent malpuech syndrome: report on three Brazilian patients with additional signs. American Journal of Medical Genetics, 58( 1), 13-17. doi:10.1002/ajmg.1320580104 -
NLM
Guion-Almeida ML. Apparent malpuech syndrome: report on three Brazilian patients with additional signs [Internet]. American Journal of Medical Genetics. 1995 ; 58( 1): 13-17.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.1320580104 -
Vancouver
Guion-Almeida ML. Apparent malpuech syndrome: report on three Brazilian patients with additional signs [Internet]. American Journal of Medical Genetics. 1995 ; 58( 1): 13-17.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.1320580104 - 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
- CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients
- Acrocallosal syndrome: report of a Brazilian girl
- Postaxial acrofacial dysostosis: report on two patients
- Hypertelorism: interobital growth, measurements, and pathogenetic considerations
- Sindrome de fraser. Relato de um caso
- Brachmann-De Lange syndrome in a mother and daughter
- Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition
- Mental and growth retardation, microtrigonocephaly, cleft palate and preauricular skin tags: a variant of the C syndrome or a new autosomal recessive syndrome?
- Atypical postaxial acrofacial dysostosis (AFD): diabetic embryopathy or a new afd syndrome?
Informações sobre o DOI: 10.1002/ajmg.1320580104 (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas