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Comparative genomic hybridization detects novel amplifications in fibroadenomas of the breast
(Wiley-Blackwell, 2001-01-01)
Comparative genomic hybridization analysis was performed for identification of chromosomal imbalances in 23 samples of fibroadenomas of the breast. Chromosomal gains rather than losses were a feature of these lesions. Only ...
Comparative genomic hybridization detects novel amplifications in fibroadenomas of the breast
(2001-01-01)
Comparative genomic hybridization analysis was performed for identification of chromosomal imbalances in 23 samples of fibroadenomas of the breast. Chromosomal gains rather than losses were a feature of these lesions. Only ...
Cytomorphological and Sterility Studies in Digitaria polevansii StentTítulo en español.
(University of Puerto Rico Mayagüez Campus Agricultural Experiment Station, 1969)
Genomic alterations in diffuse-type gastric cancer as shown by high-resolution comparative genomic hybridization
(Elsevier B.V., 2009-04-01)
Gastric adenocarcinoma is a serious public health concern, especially in northern Brazil. Gastric cancer call be subdivided into diffuse and intestinal types. Genetic imbalances in diffuse-type gastric cancer remain largely ...
Importancia de las alteraciones genéticas del mieloma múltipleImportance of the genetic alterations of multiple myeloma
(Centro Nacional de Información de Ciencias MédicasHematopatologia MolecularLa Habana, Cuba, 2022)
Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity
(BioMed Central, 2018)
Abstract
Background
Syndromic obesity is an umbrella term used to describe cases where obesity occurs with additional phenotypes. It often arises as part of a distinct ...
Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity
(Biomed Central Ltd, 2018)
Background: Syndromic obesity is an umbrella term used to describe cases where obesity occurs with additional phenotypes. It often arises as part of a distinct genetic syndrome with Prader-Willi syndrome being a classical ...
Alterações estruturais envolvendo o cromossomo x: impacto da inativação preferencial no fenótipo dos pacientes
(Universidade Federal de São Paulo (UNIFESP), 2016-01-07)
X-chromosome rearrangements are usually associated with distinct X inactivation patterns, which can influence in patient?s phenotype. To better understand the mechanisms involved in cell selection and the clinical consequences ...
Determinação das alterações genômicas em pacientes com malformações congênitas
(Universidade Estadual Paulista (Unesp), 2018-11-09)
As ACs são alterações visíveis nos cromossomos, classificadas como numéricas e estruturais. Atualmente o grande desafio da genética clínica é classificar e associar a relevância clínica dos desequilíbrios genéticos ao ...