Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder (2015)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Subjects: CITOGENÉTICA; DEFICIÊNCIA MENTAL; DOENÇAS NEONATAIS E ANORMALIDADES
- Language: Inglês
- Imprenta:
- Publisher: FMRP-USP
- Publisher place: Ribeirão Preto
- Date published: 2015
- Source:
- Título: Abstracts
- Conference titles: Workshop do Programa de Pós-Graduação em Genética
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ABNT
GENNARO, F. G. O. et al. Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder. 2015, Anais.. Ribeirão Preto: FMRP-USP, 2015. . Acesso em: 24 jan. 2026. -
APA
Gennaro, F. G. O., Gomes, A. G., Josahkian, J. A., Pontes, S. E., Laureano, L. A. F., Santos, S. A., et al. (2015). Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder. In Abstracts. Ribeirão Preto: FMRP-USP. -
NLM
Gennaro FGO, Gomes AG, Josahkian JA, Pontes SE, Laureano LAF, Santos SA, Squire JA, Martelli LR. Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder. Abstracts. 2015 ;[citado 2026 jan. 24 ] -
Vancouver
Gennaro FGO, Gomes AG, Josahkian JA, Pontes SE, Laureano LAF, Santos SA, Squire JA, Martelli LR. Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder. Abstracts. 2015 ;[citado 2026 jan. 24 ] - Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization
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- Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement
- Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family
- High resolution mapping of 12p in a patient with a mild phenotype of Pallister-Killian syndrome indicates duplication by interstitial gain of 12p11.21-p13.31
- High resolution array-CGH analysis of apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes
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