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D A Hopkinson

Showing results (91-100 of 148) with videos related to

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Journal of Medical Genetics|February 1, 1989
Rhodanese isozymes in three subjects with Leber's optic neuropathyD B Whitehouse, C J Poole, P R Kind, et al.
Animal Genetics|June 23, 2001
The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breedsK Haworth, M Breen, M Binns, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 1, 1990
Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiencyJ A Duley, H A Simmonds, D A Hopkinson, et al.
Journal of Medical Genetics|February 1, 1983
Acetylator phenotypes in Papua New GuineaR J Penketh, S F Gibney, G T Nurse, et al.
Annals of Human Genetics|October 1, 1991
Antigenic analysis of the major human phosphoglucomutase isozymes: PGM1, PGM2, PGM3 and PGM4G A Drago, D A Hopkinson, S A Westwood, et al.
Birth Defects Original Article Series|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Cytogenetics and Cell Genetics|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
A COL3A1 glycine 1006 to glutamic acid substitution in a patient with Ehlers-Danlos syndrome type IV detected by denaturing gradient gel electrophoresisP H Johnson, A J Richards, F M Pope, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Adenosine deaminase activity in a series of 19 patients with the Diamond-Blackfan syndromeD B Whitehouse, D A Hopkinson, A J Pilz, et al.
Annals of Human Genetics|October 1, 1985
Analysis of genetic variation in two human thyroxine-binding plasma proteins by immunodetection after isoelectric focusingD B Whitehouse, D A Hopkinson, A V Hill, et al.
Pageof 15

Showing results (91-100 of 148) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|February 1, 1989
Rhodanese isozymes in three subjects with Leber's optic neuropathyD B Whitehouse, C J Poole, P R Kind, et al.
Animal Genetics|June 23, 2001
The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breedsK Haworth, M Breen, M Binns, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 1, 1990
Inosine triphosphate pyrophosphohydrolase deficiency in a kindred with adenosine deaminase deficiencyJ A Duley, H A Simmonds, D A Hopkinson, et al.
Journal of Medical Genetics|February 1, 1983
Acetylator phenotypes in Papua New GuineaR J Penketh, S F Gibney, G T Nurse, et al.
Annals of Human Genetics|October 1, 1991
Antigenic analysis of the major human phosphoglucomutase isozymes: PGM1, PGM2, PGM3 and PGM4G A Drago, D A Hopkinson, S A Westwood, et al.
Birth Defects Original Article Series|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Cytogenetics and Cell Genetics|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
A COL3A1 glycine 1006 to glutamic acid substitution in a patient with Ehlers-Danlos syndrome type IV detected by denaturing gradient gel electrophoresisP H Johnson, A J Richards, F M Pope, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Adenosine deaminase activity in a series of 19 patients with the Diamond-Blackfan syndromeD B Whitehouse, D A Hopkinson, A J Pilz, et al.
Annals of Human Genetics|October 1, 1985
Analysis of genetic variation in two human thyroxine-binding plasma proteins by immunodetection after isoelectric focusingD B Whitehouse, D A Hopkinson, A V Hill, et al.
Pageof 15