Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. SHORT REPORT
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2000.02389.x/fullpdf
Reference11 articles.
1. Factor IX gene haplotypes in Brazilian Blacks and characterization of unusual Ddel alleles
2. 1 The molecular basis of haemophilia A and B
3. Haemophilia B: database of point mutations and short additions and deletions--eighth edition
4. Laboratory methods for the genetic diagnosis of bleeding disorders
5. Haemophilia B Brandenberg-type promoter mutation
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3. MUTATIONAL PROFILES OF F8 AND F9 IN A COHORT OF HAEMOPHILIA A AND HAEMOPHILIA B PATIENTS IN THE MULTI-ETHNIC MALAYSIAN POPULATION;Mediterranean Journal of Hematology and Infectious Diseases;2018-09-01
4. Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes;Thrombosis and Haemostasis;2017
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