Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement (2016)
- Authors:
- USP affiliated authors: SQUIRE, JEREMY ANDREW - FMRP ; MARTELLI, LUCIA REGINA - FMRP
- Unidade: FMRP
- Subjects: CITOGENÉTICA; ANORMALIDADES CROMOSSÔMICAS; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher: FMRP-USP
- Publisher place: Ribeirão Preto
- Date published: 2016
- Source:
- Título do periódico: Abstracts
- Conference titles: Workshop de Pós-Graduação em Genética
-
ABNT
GRANGEIRO, Carlos Henrique Paiva et al. Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement. 2016, Anais.. Ribeirão Preto: FMRP-USP, 2016. . Acesso em: 18 abr. 2024. -
APA
Grangeiro, C. H. P., Joaquim, T. M., Genaro, F. G. O., Gomes, A. G., Santos, S. A., Huber, J., et al. (2016). Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement. In Abstracts. Ribeirão Preto: FMRP-USP. -
NLM
Grangeiro CHP, Joaquim TM, Genaro FGO, Gomes AG, Santos SA, Huber J, Squire JA, Martelli LR. Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement. Abstracts. 2016 ;[citado 2024 abr. 18 ] -
Vancouver
Grangeiro CHP, Joaquim TM, Genaro FGO, Gomes AG, Santos SA, Huber J, Squire JA, Martelli LR. Karyotypy-phenotype-genotype correlation in a 4p;12q rearrangement. Abstracts. 2016 ;[citado 2024 abr. 18 ] - Phenotype-genotype correlative characterization a case of Jacobsen Syndrome without thrombocytopenia associated with a ring chromosome 11
- Chromosomal gain at an unstable region of 15q11.2 in a family with intellectual disability and behavioral disorder
- Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization
- Analysis of complex duplication-deletion (8p) rearrangement: clinical, cytogenetic and array comparative genomic characterization
- Applications of cytogenomic characterization of chromosomal rearrangements to establish a more precise phenotype-genotype correlation
- High resolution array-CGH analysis of apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes
- Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family
- Phenotype-genotype correlative characterization a case of Jacobsen Syndrome associated with a ring chromosome 11
- Genotype-phenotype correlation with ring chromosome 11
- Genotype-phenotype correlation associated with inherited homozygous paracentric inversion of chromosome 12
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
