Combined Hemophilia and Christmas Disease
Open Access
- 1 September 1964
- journal article
- research article
- Published by American Society of Hematology in Blood
- Vol. 24 (3) , 281-288
- https://doi.org/10.1182/blood.v24.3.281.281
Abstract
A case of combined hemophilia (AHG deficiency) and Christmas disease is described. Five other members of the family had either hemophilia or Christmas disease. The manner of inheritance of the two disorders was uncertain but it was considered most probable that in the mother of the combined case, coupling of the two genes had resulted from a cross-over involving the X-chromosome. It is believed that the findings are consistent with the view that the hemophilia and Christmas disease genes have quite separate loci on the X-chromosome.Keywords
This publication has 8 references indexed in Scilit:
- LINKAGE OF COLOR BLINDNESS TO HEMOPHILIAS A AND B1962
- HAEMOPHILIA IN SWEDEN .1. COAGULATION STUDIES1961
- Combined Hemophilia and PTC DeficiencyBlood, 1955
- Symposium: What Is Hemophilia?: Deuterohemophilia: Plasma Thromboplastin Factor B DeficiencyBlood, 1954
- Differentiation of Hemophilia into Two GroupsNew England Journal of Medicine, 1953
- The Thromboplastin Generation TestJournal of Clinical Pathology, 1953
- MILD HEMOPHILIA - AN ALLELIC FORM OF THE DISEASE1953
- Plasma Throinboplastin Component (PTC) Deficiency: A New Disease Resembling HemophiliaExperimental Biology and Medicine, 1952