The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy

The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy

Abstract Background The implementation of molecular karyotyping has resulted in an improved diagnostic yield in the genetic diagnostics of congenital anomalies, detected prenatally or after the termination of pregnancy. However, the systematic epidemiologic ascertainment of copy number variations in...

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Bibliographic Details
Main Authors: Gorazd Rudolf, Luca Lovrečić, Nataša Tul, Nataša Teran, Borut Peterlin
Format: Article
Language:English
Published: Wiley 2019-06-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
congenital anomalies
copy number variations
epidemiology
molecular karyotyping
termination of pregnancy
Online Access:https://doi.org/10.1002/mgg3.658

Internet

https://doi.org/10.1002/mgg3.658

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