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P C Watkins

Showing results (41-50 of 53) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1988
Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17S V Cheng, J H Nadeau, R E Tanzi, et al.
Transactions of the Association of American Physicians|January 1, 1988
Molecular genetics of the human beta-spectrin geneB G Forget, J G Chang, E Coupal, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21S E Antonarakis, S D Kittur, C Metaxotou, et al.
Genomics|August 1, 1989
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21M K McCormick, A Schinzel, M B Petersen, et al.
Nature|June 21, 1990
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8S E Lux, W T Tse, J C Menninger, et al.
American Journal of Medical Genetics|July 1, 1989
Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probesM L Van Keuren, G D Stewart, C M Bradley, et al.
The EMBO Journal|September 1, 1985
A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21S D Kittur, S E Antonarakis, R E Tanzi, et al.
Genomics|August 1, 1988
Genetic linkage map of human chromosome 21R E Tanzi, J L Haines, P C Watkins, et al.
Blood|July 1, 1988
Molecular cloning of the cDNA for human erythrocyte beta-spectrinJ C Winkelmann, T L Leto, P C Watkins, et al.
Nature|November 17, 1983
A polymorphic DNA marker genetically linked to Huntington's diseaseJ F Gusella, N S Wexler, P M Conneally, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1988
Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17S V Cheng, J H Nadeau, R E Tanzi, et al.
Transactions of the Association of American Physicians|January 1, 1988
Molecular genetics of the human beta-spectrin geneB G Forget, J G Chang, E Coupal, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21S E Antonarakis, S D Kittur, C Metaxotou, et al.
Genomics|August 1, 1989
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21M K McCormick, A Schinzel, M B Petersen, et al.
Nature|June 21, 1990
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8S E Lux, W T Tse, J C Menninger, et al.
American Journal of Medical Genetics|July 1, 1989
Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probesM L Van Keuren, G D Stewart, C M Bradley, et al.
The EMBO Journal|September 1, 1985
A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21S D Kittur, S E Antonarakis, R E Tanzi, et al.
Genomics|August 1, 1988
Genetic linkage map of human chromosome 21R E Tanzi, J L Haines, P C Watkins, et al.
Blood|July 1, 1988
Molecular cloning of the cDNA for human erythrocyte beta-spectrinJ C Winkelmann, T L Leto, P C Watkins, et al.
Nature|November 17, 1983
A polymorphic DNA marker genetically linked to Huntington's diseaseJ F Gusella, N S Wexler, P M Conneally, et al.
Pageof 6