Literature DB >> 27235911

Chromosomal Microarrays for the Prenatal Detection of Microdeletions and Microduplications.

Karen Wou1, Brynn Levy2, Ronald J Wapner3.   

Abstract

Chromosomal microarray analysis has replaced conventional G-banded karyotype in prenatal diagnosis as the first-tier test for the cytogenetic detection of copy number imbalances in fetuses with/without major structural abnormalities. This article reviews the basic technology of microarray; the value and clinical significance of the detection of microdeletions, microduplications, and other copy number variants; as well as the importance of genetic counseling for prenatal diagnosis. It also discusses the current status of noninvasive screening for some of these microdeletion and microduplication syndromes.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cell-free DNA; Copy number variant; Genetic counseling; Microarray; Microdeletion; Microduplication

Mesh:

Year:  2016        PMID: 27235911     DOI: 10.1016/j.cll.2016.01.017

Source DB:  PubMed          Journal:  Clin Lab Med        ISSN: 0272-2712            Impact factor:   1.935


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