Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations

International Journal of Immunogenetics

Volumn 34, Issue 3, 2007, Pages 143-147

  Dostal, A ^a   Linnankivi, T ^b   Somer, M ^c   Kahkonen M ^d   Litzman, J ^e   Tienari, P ^b,f  

^a HARVARD MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF HELSINKI   (Finland)

^c Vaestoliitto   (Finland)

^d TAMPERE UNIVERSITY HOSPITAL   (Finland)

^e ST ANNE S UNIVERSITY HOSPITAL   (Czech Republic)

^f HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; CHROMOSOME 18Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 18; CLINICAL ARTICLE; CORRELATION ANALYSIS; FACE DYSMORPHIA; FEMALE; FINLAND; FOOT MALFORMATION; GENE LOCUS; GENE MAPPING; GENETIC SUSCEPTIBILITY; GENOTYPE; HAND MALFORMATION; HUMAN; IMMUNOGLOBULIN A DEFICIENCY; INFECTION; MALE; MENTAL DEFICIENCY; MYELINATION; PHENOTYPE; POPULATION GENETIC PARAMETERS; PRIORITY JOURNAL; WHITE MATTER;

EID: 34248592287     PISSN: 17443121     EISSN: 1744313X     Source Type: Journal    
DOI: 10.1111/j.1744-313X.2007.00652.x     Document Type: Article

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