| Literature DB >> 27235911 |
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.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