Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization (2015)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Subjects: CITOGENÉTICA; CROMOSSOMOS HUMANOS
- Language: Inglês
- Imprenta:
- Publisher: FMRP-USP
- Publisher place: Ribeirão Preto
- Date published: 2015
- Source:
- Título do periódico: Abstracts
- Conference titles: Workshop do Programa de Pós-Graduação em Genética
-
ABNT
GRANGEIRO, C. H. P. et al. Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization. 2015, Anais.. Ribeirão Preto: FMRP-USP, 2015. . Acesso em: 28 mar. 2024. -
APA
Grangeiro, C. H. P., Gomes, A. G., Laureano, L. A. F., Joaquim, T. M., Squire, J. A., & Martelli, L. R. (2015). Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization. In Abstracts. Ribeirão Preto: FMRP-USP. -
NLM
Grangeiro CHP, Gomes AG, Laureano LAF, Joaquim TM, Squire JA, Martelli LR. Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization. Abstracts. 2015 ;[citado 2024 mar. 28 ] -
Vancouver
Grangeiro CHP, Gomes AG, Laureano LAF, Joaquim TM, Squire JA, Martelli LR. Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization. Abstracts. 2015 ;[citado 2024 mar. 28 ] - Phenotype-genotype correlative characterization a case of Jacobsen Syndrome without thrombocytopenia associated with a ring chromosome 11
- Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement
- Novas variantes de número de cópias (CNVS) na infertilidade masculina idiopática por azoospermia não obstrutiva
- High resolution array-CGH analysis apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
- 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
- Genotype-phenotype correlation of an 8p complex rearrangement
- 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
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
- Applications of cytogenomic characterization of chromosomal rearrangements to establish a more precise phenotype-genotype correlation
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