Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference17 articles.
1. The molecular basis of haemophilia B.;Lillicrap;Haemophilia,1998
2. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.;Kwon;Haemophilia,2008
3. Mutation analysis impact on the genetic counseling of sporadic hemophilia B families.;Bicocchi;Am J Med Genet A,2003
4. Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.;Koeberl;Am J Hum Genet,1990
5. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.;Attali;Thromb Haemost,1999
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