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

T Siddique

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
Genomics|May 1, 1994
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophyC Mérette, L M Brzustowicz, R J Daniels, et al.
Clinical Genetics|December 25, 2004
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genesM Faiyaz-Ul-Haque, S H E Zaidi, L M King, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
The New England Journal of Medicine|May 16, 1991
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneityT Siddique, D A Figlewicz, M A Pericak-Vance, et al.
Neurology|July 1, 1989
Linkage analysis in familial amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, B R Brooks, et al.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Neurology|August 9, 2006
Lack of association of VEGF promoter polymorphisms with sporadic ALSW Chen, M Saeed, H Mao, et al.
Brazilian Journal of Biology = Revista Brasleira De Biologia|January 19, 2022
Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplantH Faiz, O Khan, I Ali, et al.
Neurology|July 30, 2010
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, H-X Deng, N Siddique, et al.
Neurology|February 4, 2011
TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathiesC J Klein, Y Shi, F Fecto, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Genomics|May 1, 1994
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophyC Mérette, L M Brzustowicz, R J Daniels, et al.
Clinical Genetics|December 25, 2004
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genesM Faiyaz-Ul-Haque, S H E Zaidi, L M King, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
The New England Journal of Medicine|May 16, 1991
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneityT Siddique, D A Figlewicz, M A Pericak-Vance, et al.
Neurology|July 1, 1989
Linkage analysis in familial amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, B R Brooks, et al.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Neurology|August 9, 2006
Lack of association of VEGF promoter polymorphisms with sporadic ALSW Chen, M Saeed, H Mao, et al.
Brazilian Journal of Biology = Revista Brasleira De Biologia|January 19, 2022
Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplantH Faiz, O Khan, I Ali, et al.
Neurology|July 30, 2010
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaJ Yan, H-X Deng, N Siddique, et al.
Neurology|February 4, 2011
TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathiesC J Klein, Y Shi, F Fecto, et al.
Pageof 7