Hemophilia B in a 46,XX female probably caused by non-random X inactivation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb04415.x/fullpdf
Reference24 articles.
1. The gene structure of human anti-haemophilic factor IX;Anson;EMBO J,1984
2. Determination of vitamin K sensitive coagulation factors in plasma. Studies on three methods using synthetic chromogenic substrates;Bergström;Thromb Res,1978
3. Variant of factor IX deficiency in female with 45, X Turner's syndrome;Bithell;Blood,1970
4. Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-inked gene;Brown;Genomics,1990
5. Dystrophie musculaire de Duchenne chez une petite fille porteuse d'une translocation (t(X;3) (q21;ql3) de novo.;Canki;Ann Genet,1979
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1. Labor and delivery in a patient with hemophilia B;International Journal of Obstetric Anesthesia;2011-07
2. Variability in bleeding phenotype in Amish carriers of haemophilia B with the 31008 C→T mutation;Haemophilia;2009-01
3. A comparative study of X-inactivation in Rett syndrome probands and control subjects;Clinical Genetics;2008-06-28
4. Clinical manifestations and management of labor and delivery in women with factor IX deficiency*;Haemophilia;2004-09
5. Breakpoint of a balanced translocation (X:14) (q27.1;q32.3) in a girl with severe hemophilia B maps proximal to the factor IX gene;Journal of Thrombosis and Haemostasis;2004-03
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