C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects (2000)
- Authors:
- Autor USP: ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- Subjects: RETARDO MENTAL; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders
- ISSN: 1517-459X
- Volume/Número/Paginação/Ano: v. 3, n. 1, p. 5-10, Jan., 2000
-
ABNT
GUION-ALMEIDA, Maria Leine e NAKATA, Nancy Mizue Kokitsu e VENDRAMINI, Siulan. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, v. 3, n. Ja, p. 5-10, 2000Tradução . . Acesso em: 19 abr. 2024. -
APA
Guion-Almeida, M. L., Nakata, N. M. K., & Vendramini, S. (2000). C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 3( Ja), 5-10. -
NLM
Guion-Almeida ML, Nakata NMK, Vendramini S. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 5-10.[citado 2024 abr. 19 ] -
Vancouver
Guion-Almeida ML, Nakata NMK, Vendramini S. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 5-10.[citado 2024 abr. 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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- Mental and growth retardation, microtrigonocephaly, cleft palate and preauricular skin tags: a variant of the C syndrome or a new autosomal recessive syndrome?
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