Homozygous Expression of Haemophilia B in a Heterozygote
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0954-6820.1978.tb08429.x/fullpdf
Reference33 articles.
1. Spontaneous haemophilia in a genotypically normal female;Afifi;Acta Haematol,1974
2. Haemophilia A in a patient with testicular feminization;Andrejev;Thromb Diath Haemorrh,1975
3. Variant of factor IX deficiency in female with 45, X Turner's syndrome;Bithell;Blood,1970
4. Spontaneous haemophilia in a female;Braun;Thromb Diath Haemorrh,1960
5. Haemophilia A in a girl;Chapelle;Lancet,1961
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1. Genetic causes of haemophilia in women and girls;Haemophilia;2020-12-13
2. Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome;European Journal of Haematology;2009-04-24
3. Haemophilia B- in a girl;Clinical & Laboratory Haematology;2008-06-28
4. 3 Factor IX;Baillière's Clinical Haematology;1989-10
5. Severe factor viii deficiency in a chromosomally normal female;Thrombosis Research;1986-10
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