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

Peter Nürnberg

Showing results (151-160 of 517) with videos related to

Pageof 52
Sort By:
Brain : a Journal of Neurology|June 23, 2020
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjectsLisa-Marie Niestroj, Eduardo Perez-Palma, Daniel P Howrigan, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 17, 2005
Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chipsRené Gödde, Klaus Rohde, Christian Becker, et al.
Plos One|September 17, 2013
SOX9 duplication linked to intersex in deerRegina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
American Journal of Human Genetics|August 15, 2009
X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected womenRoman A Siddiqui, Ulrike Sauermann, Janine Altmüller, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 3, 2003
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2Katarina Lehmann, Petra Seemann, Sigmar Stricker, et al.
American Journal of Human Genetics|March 31, 2009
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2Katarina Dathe, Klaus W Kjaer, Anja Brehm, et al.
Molecular Genetics & Genomic Medicine|August 13, 2013
Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani AncestryBidisha Saha, Davor Lessel, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 8, 2007
Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with auraChristian Netzer, Jan Freudenberg, Mohammad R Toliat, et al.
Human Genetics|July 16, 2011
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood groupGuntram Borck, Naseebullah Kakar, Jochen Hoch, et al.
Pageof 52

Showing results (151-160 of 517) with videos related to

Sort By:
Pageof 52
Brain : a Journal of Neurology|June 23, 2020
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjectsLisa-Marie Niestroj, Eduardo Perez-Palma, Daniel P Howrigan, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 17, 2005
Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chipsRené Gödde, Klaus Rohde, Christian Becker, et al.
Plos One|September 17, 2013
SOX9 duplication linked to intersex in deerRegina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
American Journal of Human Genetics|August 15, 2009
X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected womenRoman A Siddiqui, Ulrike Sauermann, Janine Altmüller, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 3, 2003
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2Katarina Lehmann, Petra Seemann, Sigmar Stricker, et al.
American Journal of Human Genetics|March 31, 2009
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2Katarina Dathe, Klaus W Kjaer, Anja Brehm, et al.
Molecular Genetics & Genomic Medicine|August 13, 2013
Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani AncestryBidisha Saha, Davor Lessel, Sheela Nampoothiri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 8, 2007
Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with auraChristian Netzer, Jan Freudenberg, Mohammad R Toliat, et al.
Human Genetics|July 16, 2011
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood groupGuntram Borck, Naseebullah Kakar, Jochen Hoch, et al.
Pageof 52