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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Published inAmerican journal of medical genetics. Part A Vol. 155A; no. 10; pp. 2589 - 2592
Main Authors 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 Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.10.2011
Wiley-Liss
Wiley Subscription Services, Inc
Subjects
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
Human
Dysmorphism
Multiple
Comparative genomic hybridization
Malformation
Chromosome
Patient
Congenital anomaly
Craniofacial
Developmental disorder
Complexes
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Bibliography:How to Cite this Article: Gu J, Sreenath Nagamani SC, Hopwood VL, Sanchez B, Saeidinejad Y, Ou Z, Peacock S, Grange DK, Stankiewicz P, Cheung SW. 2011. 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 Part A 155:2589-2592.
Jun Gu and Sandesh C. Sreenath Nagamani contributed equally to this work.
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ArticleID:AJMG34185
Director, MGL
How to Cite this Article: Gu J, Sreenath Nagamani SC, Hopwood VL, Sanchez B, Saeidinejad Y, Ou Z, Peacock S, Grange DK, Stankiewicz P, Cheung SW. 2011. 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 Part A 155:2589–2592.
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.34185