Severe haemophilia A in a female resulting from two de novo factor VIII mutations
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb05213.x/fullpdf
Reference22 articles.
1. A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes
2. Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counseling
3. Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation
4. Discordance in a pair of identical twin carriers of factor IX deficiency
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4. Inherited Bleeding Disorders in North Indian Children: 14 years’ Experience from a Tertiary Care Center;Indian Journal of Hematology and Blood Transfusion;2019-11-21
5. The State of Skewed X Chromosome Inactivation is Retained in the Induced Pluripotent Stem Cells from a Female with Hemophilia B;Stem Cells and Development;2017-07
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