Showing results (1-10 of 365) with videos related to
Sort By:
Pageof 37
Human Heredity|January 1, 1988
DNA polymorphisms, identified by an X-chromosome short-arm probe L 1.28 (DXS7), in different racial groupsS S Papiha, S S Bhattacharya, D F RobertsLancet (London, England)|August 29, 1987
A case of disputed maternityD F Roberts, S S Papiha, S S BhattacharyaAmerican Journal of Physical Anthropology|July 1, 1991
Population variation in molecular polymorphisms of the short arm of the human X chromosomeS S Papiha, S S Mastana, D F Roberts, et al.The National Medical Journal of India|June 6, 2018
Genomic probes in prenatal diagnosis of duchenne muscular dystrophy in Indians and ChineseS S Papiha, S S BhattacharyaHuman Genetics|April 7, 1977
Genetic variants of cytoplasmic malate dehydrogenase (MDH:EC:1.1.1.37) in populations in England and the Indian subcontinent. A new S-MDH variantS S Papiha, D F RobertsClinical Genetics|January 1, 1975
Serum alkaline phosphatase in patients with multiple sclerosisS S Papiha, D F RobertsJournal of Medical Genetics|June 1, 1989
Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy geneS S Papiha, D F Roberts, A Clarke, et al.Human Genetics|January 1, 1983
Some genetic implications of isoelectric focusing of human red cell phosphoglucomutase (PGM1) and serum protein group specific component (Gc): genetic diversity in the populations of Himachal Pradesh, IndiaS S Papiha, I White, D F RobertsClinical Genetics|December 1, 1982
Group-specific component (Gc) subtypes and schizophreniaS S Papiha, D F Roberts, L McLeishAnnals of Human Biology|March 1, 1989
Gene frequencies of Gc and PGM subtypesI White, S S Papiha, D F RobertsPageof 37