Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition (1999)
- Autores:
- Autores USP: ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Assunto: GENÉTICA MÉDICA
- Idioma: Inglês
- Resumo: Os autores descrevem uma menina brasileira apresentando sequência de holoprosencefalia, anoftalmia, apêndices pré-auriculares e hipoplasia pulmonar. Diagnóstico diferencial e aspectos clínicos e genéticos são discutidos
- Imprenta:
- Fonte:
- Título do periódico: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders
- ISSN: 1517-459X
- Volume/Número/Paginação/Ano: v. 2, n. 3, p. 19-22, July, 1999
-
ABNT
GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 2, n. 3, p. 19-22, 1999Tradução . . Acesso em: 19 set. 2024. -
APA
Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 2( 3), 19-22. -
NLM
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( 3): 19-22.[citado 2024 set. 19 ] -
Vancouver
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Alobar holoprosencephaly sequence, anophthalmia, preauricular skin tags, and pulmonary hypoplasia: a previously undescribed condition. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 1999 ; 2( 3): 19-22.[citado 2024 set. 19 ] - 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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