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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1977-1-25
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pubmed:abstractText |
Chromosome analyses were made on culture lymphozytes from peripheral blood in 37 patients with humoral and local antibody deficiency syndrome. In one child with humoral IgA-deficiency a ploidymutation of sex chromosomes - a Klinefelter-Syndrome - and a structural variante of chromosome 16 were detected - karyotype 47, XXY, 16q+. No aberrations of chromosomes 18 and 21 were found out in these phenotypic completely normal children. Patients with secret-IgA-deficiency in mucosae had normal karyotypes. Theoretical aspects of possible connection of antibody deficiency syndrome and chromosomal anomalies are discussed.
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pubmed:language |
ger
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0323-4398
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
22
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
167-70
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:136884-Bacterial Infections,
pubmed-meshheading:136884-Child, Preschool,
pubmed-meshheading:136884-Chromosome Aberrations,
pubmed-meshheading:136884-Dysgammaglobulinemia,
pubmed-meshheading:136884-Female,
pubmed-meshheading:136884-Humans,
pubmed-meshheading:136884-Immunoglobulin A,
pubmed-meshheading:136884-Immunoglobulins,
pubmed-meshheading:136884-Immunologic Deficiency Syndromes,
pubmed-meshheading:136884-Infant,
pubmed-meshheading:136884-Male,
pubmed-meshheading:136884-Phenotype
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pubmed:year |
1976
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pubmed:articleTitle |
[Antibody deficiency syndrome and chromosome aberrations].
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pubmed:publicationType |
Journal Article,
English Abstract
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