Pentasomy X and hyper IgE syndrome: Co-existence of two distinct genetic disorders

European Journal of Pediatrics

Volumn 158, Issue 9, 1999, Pages 723-726

  Boeck, A ^a   Gfatter, R ^a   Braun, F ^a   Fritz, B ^b  

^a UNIVERSITY OF VIENNA   (Austria)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Hyper IgE syndrome; Pentasomy X

Indexed keywords

DNA; IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G2;

ABSCESS; ANEUPLOIDY; ARTICLE; CASE REPORT; CYTOGENETICS; ECZEMA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPERIMMUNOGLOBULINEMIA E; KARYOTYPE; MEIOSIS; NONDISJUNCTION; PENTASOMY X; PNEUMONIA; PRIORITY JOURNAL; SCHOOL CHILD; STAPHYLOCOCCUS INFECTION; X CHROMOSOME ABERRATION;

ANEUPLOIDY; CHILD; DNA; ECZEMA; FEMALE; HUMANS; IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; JOB'S SYNDROME; KARYOTYPING; MALE; MENTAL RETARDATION; MUSCULOSKELETAL ABNORMALITIES; PEDIGREE; SEX CHROMOSOME ABERRATIONS; TOOTH ABNORMALITIES; X CHROMOSOME;

EID: 0032813598     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051187     Document Type: Article

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