Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation (2007)
- Authors:
- USP affiliated authors: ALMEIDA, MARIA LEINE GUION DE - HRAC ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: HRAC; IB
- DOI: 10.1097/MCD.0b013e3280739753
- Subjects: MUTAÇÃO GENÉTICA; RETARDO MENTAL; ANORMALIDADES CRANIOFACIAIS
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Dysmorphology
- ISSN: 0962-8827
- Volume/Número/Paginação/Ano: v. 16, n. 3, p. 163-166, July 2007
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
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ABNT
CEIDE, Roseli Maria Zechi et al. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, v. 16, n. 3, p. 163-166, 2007Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3280739753. Acesso em: 30 dez. 2025. -
APA
Ceide, R. M. Z., Guion-Almeida, M. L., Rodini, E. S. de O., Oliveira, N. A. de J., & Passos-Bueno, M. R. (2007). Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation. Clinical Dysmorphology, 16( 3), 163-166. doi:10.1097/MCD.0b013e3280739753 -
NLM
Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753 -
Vancouver
Ceide RMZ, Guion-Almeida ML, Rodini ES de O, Oliveira NA de J, Passos-Bueno MR. Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutation [Internet]. Clinical Dysmorphology. 2007 ; 16( 3): 163-166.[citado 2025 dez. 30 ] Available from: https://doi.org/10.1097/MCD.0b013e3280739753 - Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?
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Informações sobre o DOI: 10.1097/MCD.0b013e3280739753 (Fonte: oaDOI API)
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