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

Hans Matsson

Showing results (21-30 of 34) with videos related to

Pageof 4
Sort By:
Nature Genetics|January 18, 2005
Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glandsMiriam Entesarian, Hans Matsson, Joakim Klar, et al.
BMC Pulmonary Medicine|November 13, 2016
Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary diseaseHans Matsson, Cilla Söderhäll, Elisabet Einarsdottir, et al.
Frontiers in Genetics|October 5, 2023
Case report: a novel deep intronic splice-altering variant in <i>DMD</i> as a cause of Becker muscular dystrophyShala Ghaderi Berntsson, Hans Matsson, Anna Kristoffersson, et al.
Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
Plos One|June 24, 2011
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neuronsSatu Massinen, Marie-Estelle Hokkanen, Hans Matsson, et al.
Journal of Human Genetics|April 17, 2015
Polymorphisms in DCDC2 and S100B associate with developmental dyslexiaHans Matsson, Mikael Huss, Helena Persson, et al.
Behavior Genetics|January 5, 2011
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populationsHans Matsson, Kristiina Tammimies, Marco Zucchelli, et al.
Human Molecular Genetics|October 4, 2018
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosisJoão Fadista, Line Skotte, Frank Geller, et al.
Human Molecular Genetics|February 21, 2007
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexiaHeidi Anthoni, Marco Zucchelli, Hans Matsson, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Nature Genetics|January 18, 2005
Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glandsMiriam Entesarian, Hans Matsson, Joakim Klar, et al.
BMC Pulmonary Medicine|November 13, 2016
Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary diseaseHans Matsson, Cilla Söderhäll, Elisabet Einarsdottir, et al.
Frontiers in Genetics|October 5, 2023
Case report: a novel deep intronic splice-altering variant in <i>DMD</i> as a cause of Becker muscular dystrophyShala Ghaderi Berntsson, Hans Matsson, Anna Kristoffersson, et al.
Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
Plos One|June 24, 2011
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neuronsSatu Massinen, Marie-Estelle Hokkanen, Hans Matsson, et al.
Journal of Human Genetics|April 17, 2015
Polymorphisms in DCDC2 and S100B associate with developmental dyslexiaHans Matsson, Mikael Huss, Helena Persson, et al.
Behavior Genetics|January 5, 2011
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populationsHans Matsson, Kristiina Tammimies, Marco Zucchelli, et al.
Human Molecular Genetics|October 4, 2018
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosisJoão Fadista, Line Skotte, Frank Geller, et al.
Human Molecular Genetics|February 21, 2007
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexiaHeidi Anthoni, Marco Zucchelli, Hans Matsson, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Pageof 4