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
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7933.2004.00626.x/fullpdf
Reference15 articles.
1. Bleeding Symptoms in Carriers of Hemophilia A and B
2. Hemophilia B in a 46,XX female probably caused by non-random X inactivation
3. Hemophilia B in a female carrier due to skewed inactivation of the normal X-chromosome
4. Variant of Factor IX Deficiency in Female with 45, X Turner’s Syndrome
5. Hemophilia B in a Phenotypically Normal Girl with XX (Ring) /XO Mosaicism
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