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Updated: Jun 28, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

Clinical and genetic analysis of a phenotypically normal three-generation family carrying 10.884 Mb deletions at

Xiao-Lin Wang1, Lin-Yuan Niu1, Yu-Jiao Wang2

  • 1Department of Medical Genetics, The Affiliated Weihai Second Municipal Hospital of Qingdao University (Weihai Maternity and Child Care Hospital), Weihai, China.

Taiwanese Journal of Obstetrics & Gynecology
|June 26, 2026
PubMed
Abstract

Keywords:
13q21.1q21.32 deletionChromosomal microarray analysis(CMA)Normal phenotypePrenatal diagnosis

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