Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization

Objective: To present prenatal diagnosis and array comparative genomic hybridization (aCGH) characterization of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) presenting with fetal ascites and ventriculomegaly in the second trimester. Case Report: A 31-year-old woman, gr...

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Bibliografische Detailangaben

Hauptverfasser:	Chih-Ping Chen, Yi-Ning Su, Richard Shih-Hung Young, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Elsevier 2010-12-01
Schriftenreihe:	Taiwanese Journal of Obstetrics & Gynecology
Schlagworte:	chromosome 16 chromosome 22 fetal ascites monosomy 22q trisomy 16p ventriculomegaly
Online-Zugang:	http://www.sciencedirect.com/science/article/pii/S1028455910601052
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