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

Thomas Meitinger

Showing results (81-90 of 536) with videos related to

Pageof 54
Sort By:
The Journal of Investigative Dermatology|December 22, 2004
A gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33Kathrin A Giehl, Gertrud N Eckstein, Anna Benet-Pagès, et al.
BMC Genomics|July 6, 2013
Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverageSandra Jansen, Bernhard Aigner, Hubert Pausch, et al.
Metabolic Brain Disease|August 10, 2016
Neonatal encephalocardiomyopathy caused by mutations in VARS2Fabian Baertling, Bader Alhaddad, Annette Seibt, et al.
Human Molecular Genetics|May 23, 2007
Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in EuropeansWerner Koch, Petra Hoppmann, Elena Michou, et al.
Metabolic Brain Disease|January 19, 2016
EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosumKatharina Danhauser, Tobias B Haack, Bader Alhaddad, et al.
American Journal of Human Genetics|September 12, 2007
Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardationJanine Wagenstaller, Stephanie Spranger, Bettina Lorenz-Depiereux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2013
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controlsMichael Zech, Nadine Gross, Angela Jochim, et al.
Genetic Epidemiology|June 21, 2012
PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypesJanina S Ried, Angela Döring, Konrad Oexle, et al.
Neuropediatrics|September 16, 2017
Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related EpilepsyMatias Wagner, Mirjana Gusic, Roman Günthner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2008
A multimetric approach to analysis of genome-wide association by single markers and composite likelihoodJane Gibson, William Tapper, David Cox, et al.
Pageof 54

Showing results (81-90 of 536) with videos related to

Sort By:
Pageof 54
The Journal of Investigative Dermatology|December 22, 2004
A gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33Kathrin A Giehl, Gertrud N Eckstein, Anna Benet-Pagès, et al.
BMC Genomics|July 6, 2013
Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverageSandra Jansen, Bernhard Aigner, Hubert Pausch, et al.
Metabolic Brain Disease|August 10, 2016
Neonatal encephalocardiomyopathy caused by mutations in VARS2Fabian Baertling, Bader Alhaddad, Annette Seibt, et al.
Human Molecular Genetics|May 23, 2007
Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in EuropeansWerner Koch, Petra Hoppmann, Elena Michou, et al.
Metabolic Brain Disease|January 19, 2016
EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosumKatharina Danhauser, Tobias B Haack, Bader Alhaddad, et al.
American Journal of Human Genetics|September 12, 2007
Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardationJanine Wagenstaller, Stephanie Spranger, Bettina Lorenz-Depiereux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2013
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controlsMichael Zech, Nadine Gross, Angela Jochim, et al.
Genetic Epidemiology|June 21, 2012
PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypesJanina S Ried, Angela Döring, Konrad Oexle, et al.
Neuropediatrics|September 16, 2017
Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related EpilepsyMatias Wagner, Mirjana Gusic, Roman Günthner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2008
A multimetric approach to analysis of genome-wide association by single markers and composite likelihoodJane Gibson, William Tapper, David Cox, et al.
Pageof 54