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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1989-4-13
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pubmed:abstractText |
The application of the intragenic probe F8 e16-19 of factor VIII gene is reported for carrier detection in preparation of prenatal diagnosis of hemophilia A in a family at risk. The proband's mother is heterozygous for the Bcl I polymorphism and prenatal diagnosis can be offered to this family.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:issn |
0323-4347
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
115
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
489-93
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:2465959-DNA Probes,
pubmed-meshheading:2465959-Female,
pubmed-meshheading:2465959-Germany, East,
pubmed-meshheading:2465959-Hemophilia A,
pubmed-meshheading:2465959-Heterozygote Detection,
pubmed-meshheading:2465959-Humans,
pubmed-meshheading:2465959-Male,
pubmed-meshheading:2465959-Pedigree,
pubmed-meshheading:2465959-Polymorphism, Genetic,
pubmed-meshheading:2465959-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:2465959-Prenatal Diagnosis
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pubmed:year |
1988
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pubmed:articleTitle |
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.
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pubmed:affiliation |
Institute of Medical Genetics, Ernst-Moritz-Arndt-University, Greifswald, GDR.
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pubmed:publicationType |
Journal Article
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