Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a non‐invasive prenatal screen positive for monosomy X
Author:
Affiliation:
1. Department of Pediatrics, Division of Human GeneticsCincinnati Children's Hospital Medical Center Cincinnati Ohio USA
2. Sequenom Laboratories San Diego California USA
3. Department of PediatricsUniversity of Cincinnati Cincinnati Ohio USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31783
Reference16 articles.
1. Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novelSHOXenhancer
2. Fetal Sex Chromosome Testing by Maternal Plasma DNA Sequencing
3. Gardner and Sutherland’s Chromosome Abnormalities and Genetic Counseling
4. Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis
5. Chromosomal mosaicism in the fetoplacental unit. Best Practice & Research;Grati F. R.;Clinical Obstetrics & Gynaecology,2017
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