Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference22 articles.
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2. Nucleotide sequence preference at rat liver and wheat germ type 1 DNA topoisomerase breakage sites in duplex SV40 DNA;Been;Nucleic Acids Res,1985
3. Copy choice illegitimate DNA recombination;Brunier;Cell,1988
4. Association of crossover points with topoisomerase I cleavage sites: A model for nonhomologous recombination;Bullock;Science,1985
5. Recurrent mutations and three novel rearrangements in the factor VIII gene of Italian descent;Casula;Blood,1990
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1. Multiplex ligation-dependent probe amplification as first mutation screening for large deletions and duplications in haemophilia;Haemophilia;2017-02-15
2. The genomic architecture of the PROS1 gene underlying large tandem duplication mutation that causes thrombophilia from hereditary protein S deficiency;Gene;2014-09
3. Intron 22 homologous regions are implicated in exons 1–22 duplications of the F8 gene;European Journal of Human Genetics;2013-01-09
4. Deep intronic variations may cause mild hemophilia A;Journal of Thrombosis and Haemostasis;2011-08
5. Characterization of duplication breakpoints in the factor VIII gene;Journal of Thrombosis and Haemostasis;2010-12
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