Educational paper : Syndromic forms of primary immunodeficiency

European Journal of Pediatrics

Volumn 170, Issue 3, 2011, Pages 295-308

  Kersseboom, Rogier ^a   Brooks, Alice ^a   Weemaes, Corry ^b  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

22q11 deletion syndrome; DNA repair disorders; Genetics; Primary immunodeficiency; Syndromic immunodeficiency

Indexed keywords

IMMUNOGLOBULIN;

ATAXIA TELANGIECTASIA; BLOOM SYNDROME; BONE MARROW TRANSPLANTATION; CARTILAGE HYPOPLASIA; CENTROMERE; CHROMOSOME DELETION 22Q11; CLINICAL FEATURE; DIGEORGE SYNDROME; DOWN SYNDROME; EARLY DIAGNOSIS; FACE DYSMORPHIA; GENETIC DISORDER; HUMORAL IMMUNE DEFICIENCY; HYPER IGE SYNDROME; HYPOHIDROTIC ECTODERMAL DYSPLASIA; IMMUNE DEFICIENCY; NIJMEGEN BREAKAGE SYNDROME; PRIMARY IMMUNE RESPONSE; PRIORITY JOURNAL; REVIEW; VELOCARDIOFACIAL SYNDROME; WISKOTT ALDRICH SYNDROME;

CHROMOSOME ABERRATIONS; DISEASE SUSCEPTIBILITY; DNA REPAIR-DEFICIENCY DISORDERS; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFECTION;

EID: 79954429958     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-011-1396-7     Document Type: Review

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