B cell development in chromosome 22q11.2 deletion syndrome

Clinical Immunology

Volumn 163, Issue , 2016, Pages 1-9

  Derfalvi, Beata ^a   Maurer, Kelly ^b   McDonald McGinn, Donna M ^b   Zackai, Elaine ^b   Meng, Wenzhao ^c   Luning Prak, Eline T ^c   Sullivan, Kathleen E ^b  

^a IWK HEALTH CENTRE   (Canada)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

22q11.2 deletion syndrome; DiGeorge syndrome; Follicular helper T cells; Immunoglobulin; Somatic hypermutation; Switched memory B cells; TBX1

Indexed keywords

IMMUNOGLOBULIN HEAVY CHAIN;

ADOLESCENT; ADULT; B LYMPHOCYTE; CHILD; COHORT ANALYSIS; DIGEORGE SYNDROME; FEMALE; FLOW CYTOMETRY; GENETIC RECOMBINATION; GENETICS; HELPER CELL; HUMAN; IMMUNOLOGY; LYMPHOCYTE ACTIVATION; MALE; PHENOTYPE; PRESCHOOL CHILD; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOMATIC HYPERMUTATION; YOUNG ADULT;

ADOLESCENT; ADULT; B-LYMPHOCYTES; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DIGEORGE SYNDROME; FEMALE; FLOW CYTOMETRY; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; LYMPHOCYTE ACTIVATION; MALE; PHENOTYPE; RECOMBINATION, GENETIC; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SOMATIC HYPERMUTATION, IMMUNOGLOBULIN; T-LYMPHOCYTES, HELPER-INDUCER; YOUNG ADULT;

EID: 84949649724     PISSN: 15216616     EISSN: 15217035     Source Type: Journal    
DOI: 10.1016/j.clim.2015.12.004     Document Type: Article

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