Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay

Am J Med Genet A. 2011 Oct;155A(10):2589-92. doi: 10.1002/ajmg.a.34185. Epub 2011 Sep 9.

Authors

Jun Gu¹, Sandesh C Sreenath Nagamani, Vicki L Hopwood, Beatriz Sanchez, Yasaman Saeidinejad, Zhishuo Ou, Sandra Peacock, Dorothy K Grange, Pawel Stankiewicz, Sau Wai Cheung

Affiliation

¹ School of Health Professions, University of Texas, MD Anderson Cancer Center, Houston, USA.

PMID: 21910221
DOI: 10.1002/ajmg.a.34185

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Abnormalities, Multiple / genetics
Abnormalities, Multiple / pathology*
Child
Chromosome Aberrations*
Chromosome Disorders / genetics*
Chromosome Disorders / pathology*
Chromosomes, Human, Pair 16 / genetics*
Comparative Genomic Hybridization
Developmental Disabilities / genetics
Developmental Disabilities / pathology*
Female
Humans