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

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Veröffentlicht in:	American journal of medical genetics. Part A 2011-10, Vol.155A (10), p.2589-2592
Hauptverfasser:	Gu, Jun, Sreenath Nagamani, Sandesh C., Hopwood, Vicki L., Sanchez, Beatriz, Saeidinejad, Yasaman, Ou, Zhishuo, Peacock, Sandra, Grange, Dorothy K., Stankiewicz, Pawel, Cheung, Sau Wai
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - genetics Abnormalities, Multiple - pathology Biological and medical sciences 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 Medical genetics Medical sciences
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