SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

Journal:
American Journal of Human Genetics
Published:
DOI:
10.1016/j.ajhg.2021.01.015
Affiliations:
11
Authors:
20
Institutions Authors Share
IRCCS Bambino Gesù Children's Hospital, Italy
7.000000
0.35
Baylor College of Medicine (BCM), United States of America (USA)
3.000000
0.15
Italy Ministry of Health, Italy
3.000000
0.15
GeneDx Inc., United States of America (USA)
3.000000
0.15
London Health Sciences Centre (LHSC), Canada
2.000000
0.10
Radboud University Medical Centre (Radboudumc), RU, Netherlands
0.500000
0.03
Donders Institute for Brain, Cognition and Behaviour, Netherlands
0.500000
0.03
The University of Manchester (UoM), United Kingdom (UK)
0.500000
0.03
Manchester Centre for Genomic Medicine (MCGM), United Kingdom (UK)
0.500000
0.03