The prevalence of genetic diagnoses in fetuses with severe congenital heart defects › Research Explorer

DOI

https://doi.org/10.1038/s41436-020-0791-8
Final published version

Amber E. L. van Nisselrooij
Malou A. Lugthart
Sally-Ann Clur
Ingeborg H. Linskens
Eva Pajkrt
Lukas A. Rammeloo
Lieke Rozendaal
Nico A. Blom
Jan M. M. van Lith
Alida C. Knegt
Mariëtte J. V. Hoffer
Emmelien Aten
Gijs W. E. Santen
Monique C. Haak

Original language	English
Pages (from-to)	1206-1214
Number of pages	9
Journal	Genetics in medicine
Volume	22
Issue number	7
Early online date	2020
DOIs	https://doi.org/10.1038/s41436-020-0791-8
Publication status	Published - 1 Jul 2020

Research areas

chromosome microarray analysis, congenital heart defects, exome sequencing, genetic syndrome, prenatal counseling

ID: 11531539