CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY)
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference11 articles.
1. Genotype assignment (carrier detection) in the haemophilias;Graham;Clin Haematol,1979
2. Molecular cloning of the gene for human anti-haemophilic factor IX;Choo;Nature,1982
3. Isolation and characterization of a c-DNA coding for human factor IX;Kurachi;Proc Natl Acad Sci USA,1982
4. Isolation of a human anti-haemophilic factor IX c-DNA clone using a unique 52 base synthetic oligonucleotide probe deduced from the ammo acid sequence of bovine factor IX;Jaye;Nucleic Acid Res,1983
5. Gene deletions in patients with haemophilia B and anti-factor IX antibodies;Giannelli;Nature,1983
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1. Assessment of heritable genetic effects using new genetic tools and sentinels in an era of personalized medicine;Environmental and Molecular Mutagenesis;2011-01-06
2. Two allotypes of factor IX present in haemophilia B;Scandinavian Journal of Haematology;2009-04-24
3. Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish families;Clinical Genetics;2008-06-28
4. Direct carrier detection in hemophilia B kindreds: Use of modified primers (mutagenic primers) for enzymatic amplification of the factor IX gene;Thrombosis Research;1991-08
5. Molekulargenetische Analysen der Hämophilie A und B;20. Hämophilie-Symposion Hamburg 1989;1990
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