Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses-Reference-Cited by-同舟云学术

Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses

Published:2020-11-13 Issue:2 Volume:185 Page:544-548
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Granadillo Jorge L.¹^ORCID,Wegner Daniel J.²,Paul Alexander J.³,Willing Marcia¹,Sisco Kathleen¹,Tedder Matthew L.⁴,Sadikovic Bekim⁵^ORCID,Wambach Jennifer A.²,Baldridge Dustin¹^ORCID,Cole Francis Sessions²,

Affiliation:

1. Division of Genetics and Genomic Medicine, Edward Mallinckrodt Department of Pediatrics Washington University School of Medicine, Saint Louis Children's Hospital Saint Louis Missouri USA

2. Division of Newborn Medicine, Edward Mallinckrodt Department of Pediatrics Washington University School of Medicine, Saint Louis Children's Hospital Saint Louis Missouri USA

3. McDonnell Genome Institute, Washington University School of Medicine Saint Louis Missouri USA

4. Greenwood Genetic Center Greenwood South Carolina USA

5. Molecular Diagnostics Division Pathology and Laboratory Medicine. London Health Sciences Centre and St. Joseph's Health Care London Ontario Canada

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61962

Reference11 articles.