Biomedical subjects
R Sanger
Publications and source records attributed to R Sanger.
Anomalous Xg inheritance with a probable explanation.
Explore the source record for details and available documents.
Two populations of Rh groups together with chromosomally abnormal cell lines in the bone marrow.
At the onset of his disease a man with polycythaemia vera had chromosomally normal cells in the bone marrow and Rh blood group CDe/cDE. Five years later he developed pancytopenia with erythroid hyperplasia of the bone marrow. This was associated with the presence of a major abnormal clone, 45,XY,B-,C-,16+, a minor clone, 45,XY,2+,3-,C-, and a few apparently normal cells. At the same time Rh blood grouping showed two populations of red cells, one CDe/cDE and one giving the reactions of CDe/CDe which can be interpreted as CDe. If monosomic CDe be the correct interpretation the case provides a strong hint that the Rh complex locus is sited either on the long arm of a B-group chromosome or, less probably, on an autosome of the C group.
Persistent mixed field polyagglutinability. Electrokinetic and serological aspects.
Explore the source record for details and available documents.
A new antibody, anti-Fy3, in the Duffy blood group system.
Explore the source record for details and available documents.
An inherited X-autosome translocation in man.
Explore the source record for details and available documents.
Xg groups and sex abnormalities in people of northern European ancestry.
Explore the source record for details and available documents.
The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry.
Explore the source record for details and available documents.
Some contributions of blood groups to human genetics.
Explore the source record for details and available documents.
Some contributions of blood groups to human genetics.
Explore the source record for details and available documents.
Gerbich blood group system: a useful genetic marker in certain Melanesians of Papua and New Guinea.
Explore the source record for details and available documents.
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation.
Explore the source record for details and available documents.
Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes.
Explore the source record for details and available documents.
Xg blood-groups and clonal-origin theory of chronic myeloid leukaemia.
Explore the source record for details and available documents.
[The gene complex DIV (C)-].
Explore the source record for details and available documents.
Xg and sex-chromosome abnormalities.
Explore the source record for details and available documents.
The red cell phenotype En(a-) and anti-Ena: serological and physicochemical aspects.
Explore the source record for details and available documents.