Molecular- and flow cytometry-based diagnosis of primary immunodeficiency disorders

Current Allergy and Asthma Reports

Volumn 10, Issue 6, 2010, Pages 460-467

  Oliveira, Joao B ^a   Fleisher, Thomas A ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

Diagnosis; Flow cytometry; Genetics; Molecular; Primary immunodeficiency

Indexed keywords

T LYMPHOCYTE RECEPTOR;

AGAMMAGLOBULINEMIA; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; CHRONIC GRANULOMATOUS DISEASE; COMMON VARIABLE IMMUNODEFICIENCY; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; DISEASE PREDISPOSITION; FLOW CYTOMETRY; GENETIC ASSOCIATION; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HUMAN; HYPER IGM SYNDROME; IMMUNE DEFICIENCY; INTERMETHOD COMPARISON; IPEX SYNDROME; LEUKOCYTE ADHESION DEFICIENCY; LEUKOCYTE ADHESION DEFICIENCY TYPE 1; LYMPHOCYTE DIFFERENTIATION; LYMPHOPROLIFERATIVE DISEASE; MUTATIONAL ANALYSIS; MYCOBACTERIOSIS; PRIMARY IMMUNE RESPONSE; REVIEW; SENSITIVITY AND SPECIFICITY; SEVERE COMBINED IMMUNODEFICIENCY; WISKOTT ALDRICH SYNDROME; X CHROMOSOME LINKED DISORDER;

FLOW CYTOMETRY; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES;

EID: 78049259067     PISSN: 15297322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11882-010-0137-8     Document Type: Review

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