Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review

Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review

Objective: Chromosome 16p11.2 deletions have been recognized as a genetic disorder with well-described postnatal phenotypes. However, the prenatal manifestations are atypical for lacking of enough evidence. Case report: Four pregnant women underwent amniocentesis for cytogenetic analysis and chromos...

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Bibliographic Details
Main Authors:	Fagui Yue, Qi Xi, Xinyue Zhang, Yuting Jiang, Hongguo Zhang, Ruizhi Liu
Format:	Article
Language:	English
Published:	Elsevier 2022-05-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Subjects:	Prenatal 16p11.2 microdeletion Chromosomal microarray analysis Phenotypic diversities Preimplantation genetic testing
Online Access:	http://www.sciencedirect.com/science/article/pii/S102845592200095X

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