Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood
Author:
Affiliation:
1. Prenatal Diagnosis Unit, Boai Hospital of Zhongshan, Zhongshan, Guangdong, China;
2. Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center, Guangzhou Medical College, Guangzhou, Guangdong, China
Funder
Science and Technology Department of Guangdong Province
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology
Link
https://www.tandfonline.com/doi/pdf/10.1080/01443615.2018.1439905
Reference10 articles.
1. Trisomy 9: Review and report of two new cases
2. Presenting physical characteristics, medical conditions, and developmental status of long-term survivors with trisomy 9 mosaicism
3. aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis
4. Chromosomal mosaicism in the fetoplacental unit
5. Revised guidelines for the diagnosis of mosaicism in amniocytes
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