Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter] (2003)
- Autores:
- Autor USP: ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- Assunto: ANORMALIDADES MÚLTIPLAS
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: American Journal of Medical Genetics
- ISSN: 0148-7299
- Volume/Número/Paginação/Ano: v. 117, n. 1, p. 84-83, Feb., 2003
-
ABNT
GUION-ALMEIDA, Maria Leine e NAKATA, Nancy Mizue Kokitsu. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics, v. 117, n. 1, p. 84-83, 2003Tradução . . Acesso em: 28 mar. 2024. -
APA
Guion-Almeida, M. L., & Nakata, N. M. K. (2003). Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics, 117( 1), 84-83. -
NLM
Guion-Almeida ML, Nakata NMK. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics. 2003 ; 117( 1): 84-83.[citado 2024 mar. 28 ] -
Vancouver
Guion-Almeida ML, Nakata NMK. Aural atresia, microtia, complex heart defect, and hearing loss syndrome: additional case [Research Letter]. American Journal of Medical Genetics. 2003 ; 117( 1): 84-83.[citado 2024 mar. 28 ] - 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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