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Comparative genomic hybridization analysis detects frequent over-representation of DNA sequences at 3q, 7p, and 8q in head and neck carcinomas
(Elsevier B.V., 2000-05-01)
Comparative genomic hybridization (CGH) was used to identify chromosomal imbalances in 19 samples of squamous cell carcinoma of the head and neck (HNSCC). The chromosome arms most often or er-represented were 3q (48%), 8q ...
Comparative genomic hybridization analysis detects frequent over-representation of DNA sequences at 3q, 7p, and 8q in head and neck carcinomas
(Elsevier B.V., 2000-05-01)
Comparative genomic hybridization (CGH) was used to identify chromosomal imbalances in 19 samples of squamous cell carcinoma of the head and neck (HNSCC). The chromosome arms most often or er-represented were 3q (48%), 8q ...
Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation
(2008)
A family with six alive patients with partial monosomy 5p and five with partial trisomy 5p due to a t(5;15)(p13.3;p12) translocation is reported. The translocation was present in four generations with eight balanced carriers. ...
Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation
(Springer, 2008-11-01)
A family with six alive patients with partial monosomy 5p and five with partial trisomy 5p due to a t(5;15)(p13.3;p12) translocation is reported. the translocation was present in four generations with eight balanced carriers. ...
CYP1A1 *2B and *4 polymorphisms are associated with lung cancer susceptibility in Mexican patients
(2013)
We compiled 104 constitutional de novo or sporadic rearranged chromosomes mimicking recombinants from a parental pericentric inversion in order to comment on their occurrence and parental derivation, meiotic or postzygotic ...
Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses
(Funpec-editoraRibeirao PretoBrasil, 2011)
Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes
(BioMed Central Ltd.London, 2014-10-31)
Background
Certain rare syndromes with developmental delay or intellectual disability caused by genomic copy number variants (CNVs), either deletions or duplications, are associated with higher rates of obesity. Current ...
Hibridação genômica comparativa (CGH) em neoplasias gástricas de indivíduos do estado do Pará
(Universidade Federal de São Paulo (UNIFESP), 2009-01-28)
Gastric adenocarcinoma is a serious public health concern, especially in the Northern Brazil. Gastric cancer can be subdivided into diffuse-type and intestinal-type. Genetic imbalances in diffuse-type gastric cancer remain ...