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 acesso aberto
- Este artigo NÃO é de acesso aberto
-
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: 12 fev. 2026. -
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 2026 fev. 12 ] 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 2026 fev. 12 ] Available from: https://doi.org/10.1159/000354095 - Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly
- Análise do gene ZIC2 em pacientes brasileiros com espectro da holoprosencefalia
- Análise do gene modificador GAS1 em pacientes com holoprosencefalia
- Relato de uma microduplicação na região 22Q11
- Noonan syndrome in diverse populations
- Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
- Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families
- Acheiropodia: report on four new Brazilian patients
- Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures
- Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
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
