Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Objective: To characterize a prenatally detected chromosomal aberration with molecular cytogenetic approaches and explore its relationship with Beckwith–Wiedemann syndrome (BWS). Case report: A 33-year-old woman, gravida 2, para 0, was referred to our prenatal clinic at 20+ weeks due to an abnormal...

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Bibliographic Details

Published in:	Taiwanese Journal of Obstetrics & Gynecology
Main Authors:	Kuan Ju Chen, Yu Mei Liu, Chien Hong Li, Yao Lung Chang, Shuenn Dyh Chang
Format:	Article
Language:	English
Published:	Elsevier 2016-12-01
Subjects:	array comparative genomic hybridization Beckwith–Wiedemann syndrome karyotyping short tandem repeat marker
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455916302030