Carrier analysis of a moderately affected haemophilia B family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2000.00452.x/fullpdf
Reference9 articles.
1. Haemophilia B. database of point mutations and short additions and deletions - eighth edition;Giannelli;Nucl Acids Res,1998
2. Nucleotide sequence of the gene for human factor IX (anti-hemophilic factor B);Yoshitake;Biochemistry,1985
3. CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series;Chen;Hum Genet,1991
4. Carrier detection for hemophilia B. evaluation of multiple polymorphic sites;Mariani;Am J Hematol,1990
5. The varying frequencies of five DNA polymorphisms of X-linked coagulant Factor IX in eight ethnic groups;Graham;Am J Hum Genet,1991
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