Advances in carrier detection in haemophilia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.1998.440358.x/fullpdf
Reference44 articles.
1. Factor VIII gene inversions in severe haemophilia A-results of an international consortium study;Antonarakis SS and a consortium of 65 international authors;Blood,1995
2. Laboratory methods for the genetic diagnosis of bleeding disorders;Goodeve;Clin Lab Haematol
3. Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the human factor VIII gene;Lalloz;Lancet,1991
4. Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene;Lalloz;Br J Haematol,1994
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1. Hemophilia A and Hemophilia B;Consultative Hemostasis and Thrombosis;2019
2. Hemophilia A and B;Consultative Hemostasis and Thrombosis;2013
3. Thrombocytopenia and Bleeding Disorders;High Risk Pregnancy;2011
4. Identification of mutations in theF9gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B;Haemophilia;2008-09
5. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing;Thrombosis Research;2007-01
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