Can we identify <scp>WHIM</scp> in infancy? Opportunities with the public newborn screening process-Reference-Cited by-同舟云学术

Can we identify WHIM in infancy? Opportunities with the public newborn screening process

Published:2022-06 Issue:2 Volume:190 Page:215-221
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:American J of Med Genetics Pt C

Author:

Yilmaz Melis¹²^ORCID,Potts David Evan¹²,Geier Christoph³⁴,Walter Jolan E.¹²⁵^ORCID

Affiliation:

1. Division of Allergy and Immunology, Department of Pediatrics and Medicine, Morsani College of Medicine University of South Florida Tampa Florida USA

2. Division of Allergy and Immunology, Department of Pediatrics Johns Hopkins All Children's Hospital St Petersburg Florida USA

3. Department of Rheumatology and Clinical Immunology University Medical Center Freiburg Freiburg Germany

4. Center for Chronic Immunodeficiency (CCI) University Medical Center Freiburg Freiburg Germany

5. Division of Allergy and Immunology Massachusetts General Hospital for Children Boston Massachusetts USA

Funder

Jeffrey Modell Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.32002

Reference42 articles.

1. High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots

2. Reference intervals for lymphocyte subsets in preterm and term neonates without immune defects

3. Epigenetic immune cell counting in human blood samples for immunodiagnostics

4. Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

5. Recommendations for uniform definitions used in newborn screening for severe combined immunodeficiency