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N Risch

Showing results (151-160 of 162) with videos related to

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American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Nature Genetics|July 14, 1998
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitusP Concannon, K J Gogolin-Ewens, D A Hinds, et al.
Genome Research|July 4, 2001
High-throughput genotyping with single nucleotide polymorphismsK Ranade, M S Chang, C T Ting, et al.
American Journal of Hypertension|January 5, 2002
The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese originK Ranade, W H Shue, Y J Hung, et al.
Journal of Autism and Developmental Disorders|July 30, 1999
Exclusion of linkage to the HLA region in ninety multiplex sibships with autismT Rogers, L Kalaydjieva, J Hallmayer, et al.
American Journal of Medical Genetics|September 22, 1999
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autismB Salmon, J Hallmayer, T Rogers, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2001
Genetic variation in aldosterone synthase predicts plasma glucose levelsK Ranade, K D Wu, N Risch, et al.
Genome Research|May 1, 1997
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibriumL J Ozelius, J Hewett, P Kramer, et al.
American Journal of Human Genetics|July 27, 1999
A genomic screen of autism: evidence for a multilocus etiologyN Risch, D Spiker, L Lotspeich, et al.
Nature Genetics|August 1, 1996
A full genome search in multiple sclerosisG C Ebers, K Kukay, D E Bulman, et al.
Pageof 17

Showing results (151-160 of 162) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Nature Genetics|July 14, 1998
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitusP Concannon, K J Gogolin-Ewens, D A Hinds, et al.
Genome Research|July 4, 2001
High-throughput genotyping with single nucleotide polymorphismsK Ranade, M S Chang, C T Ting, et al.
American Journal of Hypertension|January 5, 2002
The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese originK Ranade, W H Shue, Y J Hung, et al.
Journal of Autism and Developmental Disorders|July 30, 1999
Exclusion of linkage to the HLA region in ninety multiplex sibships with autismT Rogers, L Kalaydjieva, J Hallmayer, et al.
American Journal of Medical Genetics|September 22, 1999
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autismB Salmon, J Hallmayer, T Rogers, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2001
Genetic variation in aldosterone synthase predicts plasma glucose levelsK Ranade, K D Wu, N Risch, et al.
Genome Research|May 1, 1997
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibriumL J Ozelius, J Hewett, P Kramer, et al.
American Journal of Human Genetics|July 27, 1999
A genomic screen of autism: evidence for a multilocus etiologyN Risch, D Spiker, L Lotspeich, et al.
Nature Genetics|August 1, 1996
A full genome search in multiple sclerosisG C Ebers, K Kukay, D E Bulman, et al.
Pageof 17