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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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Main Authors:	Chih-Ping Chen (Author), Ming Chen (Author), Yi-Ning Su (Author), Chin-Yuan Hsu (Author), Fuu-Jen Tsai (Author), Schu-Rern Chern (Author), Pei-Chen Wu (Author), Chen-Chi Lee (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2010-12-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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