Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray

This study examined the molecular characterization of a prenatal case with true fetal mosaicism of small supernumerary marker chromosome 16 (sSMC(16)). A 41-year-old female underwent amniocentesis at 19 weeks of gestation due to advanced maternal age. Chromosomal analysis for cultured amniocytes rev...

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Bibliographic Details
Main Authors: Tien-Yu Yao, Wan-Ju Wu, Kim-Seng Law, Mei-Hui Lee, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Chen, Gwo-Chin Ma
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Diagnostics
Subjects:
sSMC(16)
mosaicism
chromosome microarray analysis
chromosome 16p11.2 duplication syndrome
prenatal counseling
prenatal diagnosis
Online Access:https://www.mdpi.com/2075-4418/11/8/1457

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https://www.mdpi.com/2075-4418/11/8/1457

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