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

M Keddache

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Molecular Psychiatry|June 9, 2005
Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regressionC A Molloy, M Keddache, L J Martin
Clinical Genetics|June 7, 2003
Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationshipsH Zhao, M Keddache, L Bailey, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1997
Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31Y Tomer, G Barbesino, M Keddache, et al.
Molecular Psychiatry|December 31, 2003
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19J D Buxbaum, J Silverman, M Keddache, et al.
American Journal of Medical Genetics. Part A|September 17, 2008
Genotype-phenotype correlations in Rubinstein-Taybi syndromeE K Schorry, M Keddache, N Lanphear, et al.
Neurology|September 1, 1996
Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsyD A Greenberg, M Durner, S Shinnar, et al.
Lupus|April 5, 2012
Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiencyB Namjou, M Keddache, D Fletcher, et al.
American Journal of Human Genetics|March 21, 2000
Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsyD A Greenberg, M Durner, M Keddache, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Psychiatry|June 9, 2005
Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regressionC A Molloy, M Keddache, L J Martin
Clinical Genetics|June 7, 2003
Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationshipsH Zhao, M Keddache, L Bailey, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1997
Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31Y Tomer, G Barbesino, M Keddache, et al.
Molecular Psychiatry|December 31, 2003
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19J D Buxbaum, J Silverman, M Keddache, et al.
American Journal of Medical Genetics. Part A|September 17, 2008
Genotype-phenotype correlations in Rubinstein-Taybi syndromeE K Schorry, M Keddache, N Lanphear, et al.
Neurology|September 1, 1996
Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsyD A Greenberg, M Durner, S Shinnar, et al.
Lupus|April 5, 2012
Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiencyB Namjou, M Keddache, D Fletcher, et al.
American Journal of Human Genetics|March 21, 2000
Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsyD A Greenberg, M Durner, M Keddache, et al.
Pageof 1