Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings

Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings

Objective: To present prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 1p (1p36.23→pter) and partial trisomy 20p (20p12.1→pter) associated with ventriculomegaly, ventricular septal defect and midface hypoplasia. Materials, Methods and Results: A 31-year-old,...

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Bibliographic Details
Main Authors:	Chih-Ping Chen, Ming Chen, Yi-Ning Su, Chin-Yuan Hsu, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2010-12-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Subjects:	chromosome 1 chromosome 1p36 deletion syndrome chromosome 20 monosomy 1p36 prenatal diagnosis ultrasound
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455910601003

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