Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Objective: To present the prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation. Case Report: A 37-year-old woman, G3P1, underwent amniocentesis at 17 weeks of gestation because of her advanced maternal age. Her husband was 38 years old. Amnio...

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Bibliographic Details
Main Authors: Chih-Ping Chen, Fung-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang
Format: Article
Language:English
Published: Elsevier 2016-04-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
array comparative genomic hybridization
3p deletion
16q duplication
prenatal diagnosis
quantitative fluorescent polymerase chain reaction
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455916000504

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http://www.sciencedirect.com/science/article/pii/S1028455916000504

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