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D Viles

Showing results (11-20 of 23) with videos related to

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Nature Biotechnology|July 11, 2006
Cell type-specific delivery of siRNAs with aptamer-siRNA chimerasJames O McNamara, Eran R Andrechek, Yong Wang, et al.
American Journal of Medical Genetics|June 22, 2000
Heterogeneity in Paget disease of the boneM A Nance, F Q Nuttall, M J Econs, et al.
Clinical Genetics|October 12, 1999
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative GroupM C Speer, J Nye, D McLone, et al.
Biostatistics (Oxford, England)|March 15, 2021
Information enhanced model selection for Gaussian graphical model with application to metabolomic dataJie Zhou, Anne G Hoen, Susan Mcritchie, et al.
Genomics|November 26, 1998
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31L Bartoloni, S K Horrigan, K D Viles, et al.
American Journal of Medical Genetics|July 13, 2002
T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect familiesMarcy C Speer, Elizabeth C Melvin, Kristi D Viles, et al.
American Journal of Human Genetics|February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7M C Speer, J M Vance, J M Grubber, et al.
Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Human Molecular Genetics|July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37M C Speer, R Tandan, P N Rao, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Nature Biotechnology|July 11, 2006
Cell type-specific delivery of siRNAs with aptamer-siRNA chimerasJames O McNamara, Eran R Andrechek, Yong Wang, et al.
American Journal of Medical Genetics|June 22, 2000
Heterogeneity in Paget disease of the boneM A Nance, F Q Nuttall, M J Econs, et al.
Clinical Genetics|October 12, 1999
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative GroupM C Speer, J Nye, D McLone, et al.
Biostatistics (Oxford, England)|March 15, 2021
Information enhanced model selection for Gaussian graphical model with application to metabolomic dataJie Zhou, Anne G Hoen, Susan Mcritchie, et al.
Genomics|November 26, 1998
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31L Bartoloni, S K Horrigan, K D Viles, et al.
American Journal of Medical Genetics|July 13, 2002
T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect familiesMarcy C Speer, Elizabeth C Melvin, Kristi D Viles, et al.
American Journal of Human Genetics|February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7M C Speer, J M Vance, J M Grubber, et al.
Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Human Molecular Genetics|July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37M C Speer, R Tandan, P N Rao, et al.
Pageof 3