Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia-Reference-Cited by-同舟云学术

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Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia

Published:2018-01 Issue:2 Volume:38 Page:91-98
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Zou Zhiyong¹,Huang Linhuan¹,Lin Shaobin¹,He Zhiming¹,Zhu Hui¹,Zhang Yi¹^ORCID,Fang Qun¹,Luo Yanmin¹^ORCID

Affiliation:

1. Department of Obstetrics and Gynecology; The First Affiliated Hospital of Sun Yat-Sen University; Guangzhou People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference52 articles.

1. Evaluation of fetal central nervous system anomalies by ultrasound and its anatomical co-relation;Onkar;J Clin Diagn Res,2014

2. Cystic malformations of the posterior cranial fossa originating from a defect of the posterior membranous area. Mega cisterna magna and persisting Blake's pouch: two separate entities;Tortori-Donati;Childs Nerv Syst,1996

3. Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies;D'Antonio;Ultrasound Obstet Gynecol,2016

4. Dandy-Walker malformation: a review of 78 cases diagnosed by prenatal sonography;Has;Fetal Diagn Ther,2004

5. Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray;Coppinger;Prenat Diagn,2009

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