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Updated: May 21, 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

Genetic haploinsufficiency as a phenotypic determinant of a deletion 13q syndrome

Armen G Kasyan1, Kurt Benirschke

  • 1Department of Pathology, University of California-San Diego, University Medical Center, 200 West Arbor Drive, San Diego, CA 92103-8321, USA. akasyan@ucsd.edu

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
|December 6, 2005
PubMed

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