Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S F NELSON

Showing results (1-10 of 47) with videos related to

Pageof 5
Sort By:
Tennessee Medicine : Journal of the Tennessee Medical Association|June 14, 2001
An unusual cause of pelvic massS F Nelson
Electrophoresis|February 1, 1995
Genomic mismatch scanning: current progress and potential applicationsS F Nelson
Genomics|February 18, 1998
Genomic mismatch scanning identifies human genomic DNA shared identical by descentV G Cheung, S F Nelson
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNAV G Cheung, S F Nelson
The Journal of Speech Disorders|October 29, 2010
Stuttering in twin typesS F NELSON, N HUNTER, M WALTER
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|November 21, 2001
Biclonal bacteremia due to Stenotrophomonas maltophilia in a cancer patientA Lechner, J F Hindler, S F Nelson
Genetic Analysis : Biomolecular Engineering|October 1, 1996
A biotinylated MutS fusion protein and its use in a rapid mutation screening techniqueD H Geschwind, R Rhee, S F Nelson
Annals of Neurology|July 17, 1998
The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementiaD Geschwind, J Karrim, S F Nelson, et al.
American Journal of Human Genetics|November 5, 1997
Progressive ataxia due to a missense mutation in a calcium-channel geneQ Yue, J C Jen, S F Nelson, et al.
Annals of Neurology|January 1, 1997
Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19pR W Baloh, Q Yue, J M Furman, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Tennessee Medicine : Journal of the Tennessee Medical Association|June 14, 2001
An unusual cause of pelvic massS F Nelson
Electrophoresis|February 1, 1995
Genomic mismatch scanning: current progress and potential applicationsS F Nelson
Genomics|February 18, 1998
Genomic mismatch scanning identifies human genomic DNA shared identical by descentV G Cheung, S F Nelson
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNAV G Cheung, S F Nelson
The Journal of Speech Disorders|October 29, 2010
Stuttering in twin typesS F NELSON, N HUNTER, M WALTER
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|November 21, 2001
Biclonal bacteremia due to Stenotrophomonas maltophilia in a cancer patientA Lechner, J F Hindler, S F Nelson
Genetic Analysis : Biomolecular Engineering|October 1, 1996
A biotinylated MutS fusion protein and its use in a rapid mutation screening techniqueD H Geschwind, R Rhee, S F Nelson
Annals of Neurology|July 17, 1998
The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementiaD Geschwind, J Karrim, S F Nelson, et al.
American Journal of Human Genetics|November 5, 1997
Progressive ataxia due to a missense mutation in a calcium-channel geneQ Yue, J C Jen, S F Nelson, et al.
Annals of Neurology|January 1, 1997
Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19pR W Baloh, Q Yue, J M Furman, et al.
Pageof 5