Molecular mechanisms underlying hemophilia A phenotype in seven females
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2009.03346.x/fullpdf
Reference40 articles.
1. Female haemophilia A: two unusual cases caused by skewed X inactivation;Knobe;Haemophilia,2008
2. Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females;Renault;Eur J Hum Genet,2007
3. Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A;Bicocchi;Eur J Hum Genet,2005
4. Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A;Valleix;Blood,2002
5. Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female;Favier;Blood,2000
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