Chromosomal microarray analysis detects trisomy 9 mosaicism in a prenatal case not revealed by conventional cytogenetic analysis of cord blood

J Obstet Gynaecol. 2019 Jan;39(1):123-125. doi: 10.1080/01443615.2018.1439905. Epub 2018 Mar 21.

Authors

Hai-Shen Tang¹, De-Gang Wang¹, Lv-Yin Huang², Dong-Zhi Li²

Affiliations

¹ a Prenatal Diagnosis Unit , Boai Hospital of Zhongshan , Zhongshan , Guangdong , China.
² b Prenatal Diagnostic Center , Guangzhou Women and Children Medical Center, Guangzhou Medical College , Guangzhou , Guangdong , China.

PMID: 29560757
DOI: 10.1080/01443615.2018.1439905

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple
Adult
Amniocentesis
Chromosomes, Human, Pair 9
Cordocentesis*
Cytogenetic Analysis
Female
Humans
Infant, Low Birth Weight
Infant, Newborn
Male
Microarray Analysis*
Mosaicism
Pregnancy
Trisomy / diagnosis*
Uniparental Disomy / diagnosis*

Supplementary concepts

Chromosome 9, trisomy mosaic