Neuropsychological assessment of a family with genodermatosis to be clarified (2011)
- Authors:
- USP affiliated authors: TABAQUIM, MARIA DE LOURDES MERIGHI - FOB ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidades: FOB; HRAC
- Subjects: AVALIAÇÃO NEUROPSICOLÓGICA; DOENÇAS HEREDITÁRIAS; DOENÇAS DA PELE E DO TECIDO CONJUNTIVO; APRENDIZAGEM
- Language: Inglês
- Imprenta:
- Publisher: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo
- Publisher place: Bauru
- Date published: 2011
- Source:
- Título: Abstracts
- Conference titles: International Meeting on Craniofacial Anomalies: Clinical Phenotype, Genes Related and New Perspectives
-
ABNT
COELHO, D. S et al. Neuropsychological assessment of a family with genodermatosis to be clarified. 2011, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2011. . Acesso em: 13 fev. 2026. -
APA
Coelho, D. S., Tabaquim, M. de L. M., Giacheti, C. M., Guion-Almeida, M. L., & Richieri-Costa, A. (2011). Neuropsychological assessment of a family with genodermatosis to be clarified. In Abstracts. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. -
NLM
Coelho DS, Tabaquim M de LM, Giacheti CM, Guion-Almeida ML, Richieri-Costa A. Neuropsychological assessment of a family with genodermatosis to be clarified. Abstracts. 2011 ;[citado 2026 fev. 13 ] -
Vancouver
Coelho DS, Tabaquim M de LM, Giacheti CM, Guion-Almeida ML, Richieri-Costa A. Neuropsychological assessment of a family with genodermatosis to be clarified. Abstracts. 2011 ;[citado 2026 fev. 13 ] - Newly recognized autosomal recessive MCA/MR/overgrowth syndrome
- Severe midline craniofacial anomalies: overlap with Pai syndrome
- O serviço de genética clínica no HRAC/USP
- Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?
- Nonsyndromic alar clefts: report of five brazilian patients
- Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause
- Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family
- Pai syndrome: report of seven south american patients
- Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type
- Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
