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

J Hallmayer

Showing results (51-60 of 68) with videos related to

Pageof 7
Sort By:
Molecular Psychiatry|August 23, 2002
APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory lossS M Laws, R M Clarnette, K Taddei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathyF L Mastaglia, K J Nowak, R Stell, et al.
Schizophrenia Research|May 1, 1996
Genetic relationship between dopamine transporter gene and schizophrenia: linkage and associationW Maier, J Minges, N Eckstein, et al.
American Journal of Human Genetics|October 3, 1998
Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysisS G Schwab, J Hallmayer, B Lerer, et al.
American Journal of Medical Genetics|July 23, 1998
Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysisS G Schwab, J Hallmayer, M Albus, et al.
Archives of General Psychiatry|November 1, 1996
Autism and the X chromosome. Multipoint sib-pair analysisJ Hallmayer, J M Hebert, D Spiker, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Searching for susceptibility genes in schizophrenia by genetic linkage analysisD B Wildenauer, J Hallmayer, S G Schwab, et al.
Molecular Psychiatry|December 29, 2000
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6S G Schwab, J Hallmayer, M Albus, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Molecular Psychiatry|July 8, 1999
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents triosO Wittekindt, S G Schwab, E Burgert, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Molecular Psychiatry|August 23, 2002
APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory lossS M Laws, R M Clarnette, K Taddei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 17, 1999
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathyF L Mastaglia, K J Nowak, R Stell, et al.
Schizophrenia Research|May 1, 1996
Genetic relationship between dopamine transporter gene and schizophrenia: linkage and associationW Maier, J Minges, N Eckstein, et al.
American Journal of Human Genetics|October 3, 1998
Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysisS G Schwab, J Hallmayer, B Lerer, et al.
American Journal of Medical Genetics|July 23, 1998
Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysisS G Schwab, J Hallmayer, M Albus, et al.
Archives of General Psychiatry|November 1, 1996
Autism and the X chromosome. Multipoint sib-pair analysisJ Hallmayer, J M Hebert, D Spiker, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Searching for susceptibility genes in schizophrenia by genetic linkage analysisD B Wildenauer, J Hallmayer, S G Schwab, et al.
Molecular Psychiatry|December 29, 2000
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6S G Schwab, J Hallmayer, M Albus, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Molecular Psychiatry|July 8, 1999
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents triosO Wittekindt, S G Schwab, E Burgert, et al.
Pageof 7