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Paper Details

Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.
J Allergy Clin Immunol
11
2022
SASH3, SASH3-, copy number variants, immune-associated genes, immunodeficiency, inborn errors of immunity, participant, participants, patients
Author NameAffiliation
Morgan SimilukNational Institute of Allergy and Infectious Diseases
Joie DavisLaboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases
Leila JamalCenter for Cancer Research, National Cancer Institute, National Institutes of Health Clinical Center, Md Johns Hopkins/NIH Genetic Counseling Training Program
Joshua D MilnerInstitute of Genomic Medicine, Columbia University
Jennifer J JohnstonCenter for Precision Health Research, National Human Genome Research Institute
Jennifer J JohnstonCenter for Precision Health Research, National Human Genome Research Institute
Eric KarlinsNational Institute of Allergy and Infectious Diseases
Sergio D RosenzweigNational Institutes of Health Clinical Center
Weimin Bi
Melody C CarterNational Institute of Allergy and Infectious Diseases
Amy D KlionNational Institute of Allergy and Infectious Diseases
Jenna R E BergersonPrimary Immune Deficiency Clinic (Autoimmune Lymphoproliferative Syndrome Clinic), Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases
Leslie G BieseckerCenter for Precision Health Research, National Human Genome Research Institute
Leslie G BieseckerCenter for Precision Health Research, National Human Genome Research Institute
Luigi D NotarangeloLaboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases
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