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D A Hopkinson

Showing results (131-140 of 148) with videos related to

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Annals of Human Genetics|October 1, 1983
A genetic polymorphism of a human urinary mucinS Karlsson, D M Swallow, B Griffiths, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood samplingG Corney, D B Whitehouse, D A Hopkinson, et al.
Experimental and Clinical Immunogenetics|January 1, 1991
Identification of a conserved epitope in class I alcohol dehydrogenase isoenzymes using monoclonal antibodiesA Adinolfi, N Leone, D Swallow, et al.
Human Genetics|July 27, 1976
The occurrence of Hb E Saskatoon in ScotlandD Tills, V Muir, A Warlow, et al.
Annals of Human Genetics|January 1, 1984
The human glutathione S-transferases: studies on the tissue distribution and genetic variation of the GST1, GST2 and GST3 isozymesR C Strange, C G Faulder, B A Davis, et al.
Biochemical Genetics|December 1, 1985
The human glutathione S-transferases: developmental aspects of the GST1, GST2, and GST3 lociR C Strange, B A Davis, C G Faulder, et al.
Hepatology (Baltimore, Md.)|August 1, 1990
HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiencyD G Doherty, P T Donaldson, D B Whitehouse, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1D B Whitehouse, W Putt, J U Lovegrove, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombinationR E March, W Putt, M Hollyoake, et al.
Journal of Medical Genetics|June 1, 1979
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosisA G Whitelaw, P A Rogers, D A Hopkinson, et al.
Pageof 15

Showing results (131-140 of 148) with videos related to

Sort By:
Pageof 15
Annals of Human Genetics|October 1, 1983
A genetic polymorphism of a human urinary mucinS Karlsson, D M Swallow, B Griffiths, et al.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood samplingG Corney, D B Whitehouse, D A Hopkinson, et al.
Experimental and Clinical Immunogenetics|January 1, 1991
Identification of a conserved epitope in class I alcohol dehydrogenase isoenzymes using monoclonal antibodiesA Adinolfi, N Leone, D Swallow, et al.
Human Genetics|July 27, 1976
The occurrence of Hb E Saskatoon in ScotlandD Tills, V Muir, A Warlow, et al.
Annals of Human Genetics|January 1, 1984
The human glutathione S-transferases: studies on the tissue distribution and genetic variation of the GST1, GST2 and GST3 isozymesR C Strange, C G Faulder, B A Davis, et al.
Biochemical Genetics|December 1, 1985
The human glutathione S-transferases: developmental aspects of the GST1, GST2, and GST3 lociR C Strange, B A Davis, C G Faulder, et al.
Hepatology (Baltimore, Md.)|August 1, 1990
HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiencyD G Doherty, P T Donaldson, D B Whitehouse, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1D B Whitehouse, W Putt, J U Lovegrove, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombinationR E March, W Putt, M Hollyoake, et al.
Journal of Medical Genetics|June 1, 1979
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosisA G Whitelaw, P A Rogers, D A Hopkinson, et al.
Pageof 15