Pages that link to "Q35912273"
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The following pages link to Linkage of color blindness to hemophilias A and B. (Q35912273):
Displaying 12 items.
- Genetics of human blood coagulation (Q33585242) (← links)
- The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3. (Q33931052) (← links)
- Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes (Q35199665) (← links)
- Phenotypic diversity of human diseases resulting from allelic series (Q35569756) (← links)
- X CHROMOSOME MAPPING OF GENES FOR RED-GREEN COLORBLINDNESS AND XG (Q35912355) (← links)
- THE LINKAGE RELATIONS OF HEMOPHILIA A AND HEMOPHILIA B (CHRISTMAS DISEASE) TO THE XG BLOOD GROUP SYSTEM (Q35912870) (← links)
- Linkage Between the X Chromosome Loci for Glucose-6-Phosphate Dehydrogenase Electrophoretic Variation and Hemophilia A. (Q35912980) (← links)
- Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). (Q36247458) (← links)
- Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site (Q37580477) (← links)
- Combined hereditary deficiency of the sixth component of complement and factor VIII coagulant activity in a Dutch family (Q45864417) (← links)
- Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome). (Q52090614) (← links)
- Regional localization of the human factor IX gene by molecular hybridization (Q71240068) (← links)