Improved criterion-referenced assessment in indirect tracking of haemophilia A using a 0.23 cM-resolution dense polymorphic marker set
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2009.02056.x/fullpdf
Reference28 articles.
1. Characterization of the human factor VIII gene;Gitschier;Nature,1984
2. Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene;Lalloz;Lancet,1991
3. Haemophilia A diagnosis by automated fluorescent DNA detection of ten factor VIII intron 13 dinucleotide repeat alleles;Kochhan;Blood Coagul Fibrinolysis,1994
4. Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene;Lalloz;Br J Haematol,1994
5. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection;Machado;Haemophilia,2009
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1. Single‐tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb fromF8for simplified preimplantation genetic diagnosis of hemophilia A;Journal of Thrombosis and Haemostasis;2017-04-28
2. Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families;Blood Coagulation & Fibrinolysis;2015-03
3. 5meCpG Epigenetic Marks Neighboring a Primate-Conserved Core Promoter Short Tandem Repeat Indicate X-Chromosome Inactivation;PLoS ONE;2014-07-31
4. Accurate tracking genetic markers in haemophilia linkage analysis: a matter beyond scientific priority;Haemophilia;2012-05-28
5. Informativeness of a novel multiallelic marker-set comprising an F8 intron 21 and three tightly linked loci for haemophilia A carriership analysis;Haemophilia;2010-11-11
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