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Journal of Medical Genetics
|
December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding study
S Karlsson, B Griffiths, D M Swallow, et al.
Biochemical Genetics
|
October 1, 1979
Characterization of human carbonic anhydrase III from skeletal muscle
N Carter, S Jeffery, A Shiels, et al.
Annals of Human Genetics
|
July 1, 1970
Genetically determined electrophoretic variants of human red cell NADH diaphorase
D A Hopkinson, G Corney, P J Cook, et al.
Oncogene
|
October 18, 2006
Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cells
S E Aiyar, A L Blair, D A Hopkinson, et al.
Annals of Human Genetics
|
October 1, 1977
An interpretation of human diaphorase isozymes in terms of three gene loci DIA1, DIA2 and DIA3
R A Fisher, Y H Edwards, W Putt, et al.
Annals of Human Genetics
|
May 1, 1985
Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3
I Santisteban, S Povey, L F West, et al.
Prenatal Diagnosis
|
April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases
C M Abbott, J U Lovegrove, D B Whitehouse, et al.
Birth Defects Original Article Series
|
January 1, 1976
Family studies on esterase D and chromosome 13 in man
E B Robson, D A Hopkinson, K E Buckton, et al.
Molecular Biology and Evolution
|
April 29, 1998
A phylogenetic approach to the identification of phosphoglucomutase genes
D B Whitehouse, J Tomkins, J U Lovegrove, et al.
Prenatal Diagnosis
|
June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases
C M Abbott, J U Lovegrove, D B Whitehouse, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 148) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
December 1, 1984
Glycoproteins in cystic fibrosis: a lectin binding study
S Karlsson, B Griffiths, D M Swallow, et al.
Biochemical Genetics
|
October 1, 1979
Characterization of human carbonic anhydrase III from skeletal muscle
N Carter, S Jeffery, A Shiels, et al.
Annals of Human Genetics
|
July 1, 1970
Genetically determined electrophoretic variants of human red cell NADH diaphorase
D A Hopkinson, G Corney, P J Cook, et al.
Oncogene
|
October 18, 2006
Regulation of clustered gene expression by cofactor of BRCA1 (COBRA1) in breast cancer cells
S E Aiyar, A L Blair, D A Hopkinson, et al.
Annals of Human Genetics
|
October 1, 1977
An interpretation of human diaphorase isozymes in terms of three gene loci DIA1, DIA2 and DIA3
R A Fisher, Y H Edwards, W Putt, et al.
Annals of Human Genetics
|
May 1, 1985
Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3
I Santisteban, S Povey, L F West, et al.
Prenatal Diagnosis
|
April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases
C M Abbott, J U Lovegrove, D B Whitehouse, et al.
Birth Defects Original Article Series
|
January 1, 1976
Family studies on esterase D and chromosome 13 in man
E B Robson, D A Hopkinson, K E Buckton, et al.
Molecular Biology and Evolution
|
April 29, 1998
A phylogenetic approach to the identification of phosphoglucomutase genes
D B Whitehouse, J Tomkins, J U Lovegrove, et al.
Prenatal Diagnosis
|
June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases
C M Abbott, J U Lovegrove, D B Whitehouse, et al.
Page
of 15