Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-Mb distal microduplication at 22q11.2 (2013)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; LEGNARO, CHIARA DE CAMPOS - HRAC
- Unidade: HRAC
- DOI: 10.1159/000354095
- Subjects: TRANSTORNOS COGNITIVOS; TRANSTORNOS DE APRENDIZAGEM; LÁBIO FISSURADO; ANORMALIDADES CRANIOFACIAIS
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular Syndromology
- ISSN: 1661-8769
- Volume/Número/Paginação/Ano: v. 4, n. 6, p. 292-296, Sept. 2013
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
-
ABNT
BICUDO, Lucilene Arilho Ribeiro et al. Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-Mb distal microduplication at 22q11.2. Molecular Syndromology, v. 4, n. 6, p. 292-296, 2013Tradução . . Disponível em: https://doi.org/10.1159/000354095. Acesso em: 06 nov. 2024. -
APA
Bicudo, L. A. R., LEGNARO, C. H. I. A. R. A. D. E. C. A. M. P. O. S., Gamba, B. F., Sandri, R. M. C. de S., & Richieri-Costa, A. (2013). Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-Mb distal microduplication at 22q11.2. Molecular Syndromology, 4( 6), 292-296. doi:10.1159/000354095 -
NLM
Bicudo LAR, LEGNARO CHIARADECAMPOS, Gamba BF, Sandri RMC de S, Richieri-Costa A. Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-Mb distal microduplication at 22q11.2 [Internet]. Molecular Syndromology. 2013 ; 4( 6): 292-296.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1159/000354095 -
Vancouver
Bicudo LAR, LEGNARO CHIARADECAMPOS, Gamba BF, Sandri RMC de S, Richieri-Costa A. Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-Mb distal microduplication at 22q11.2 [Internet]. Molecular Syndromology. 2013 ; 4( 6): 292-296.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1159/000354095 - Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
- Tibial hemimelia: report of a new brazilian family an overview
- Atypical craniofacial clefts: a syndromological approach
- A década da linguagem: os genes começam a falar
- Estudo genético-clínico de 144 pacientes portadores de deficiência auditiva não sindrômica
- Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
- Perfil audiológico de indivíduos portadores da síndrome de Goldenhar
- Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
- Variable phenotypic manifestations of a K44N mutation in the TGIF gene
- PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
Informações sobre o DOI: 10.1159/000354095 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
