Hemophilia B in a 46,XX female probably caused by non-random X inactivation
- 1 January 1993
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 43 (1) , 1-4
- https://doi.org/10.1111/j.1399-0004.1993.tb04415.x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Haemophilia in SwedenActa Medica Scandinavica, 2009
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked geneGenomics, 1990
- Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22Genomics, 1989
- Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes.Journal of Clinical Investigation, 1987
- Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.Journal of Clinical Investigation, 1987
- The Molecular Basis of Severe Hemophilia B in a GirlNew England Journal of Medicine, 1986
- Gene deletions in patients with haemophilia B and anti-factor IX antibodiesNature, 1983
- Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.Journal of Medical Genetics, 1979
- The Occurrence of Homozygous Hemophilia in the FemaleActa Haematologica, 1971