A hemophilic son of a hemophiliac: did my son inherit my hemophilia?
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2006.02294.x/fullpdf
Reference6 articles.
1. Non-random X chromosome DNA methylation patterns in hemophilic females;Nisen;J Clin Invest,1989
2. Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation;Ingerslev;Clin Genet,1989
3. Severe haemophilia A in a female: a compound heterozygote with non-random X-inactivation;Seeler;Haemophilia,1999
4. Female haemophiliac homozygous for the factor VIII intron 22 inversion mutation, with transcriptional inactivation of one of the factor VIII alleles;David;Haemophilia,2003
5. Female hemophilia A heterozygous for a de novo frameshift and a novel missense mutation of factor VIII;Cai;J Thromb Haemost,2006
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