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 Muenke

Showing results (81-90 of 104) with videos related to

Pageof 11
Sort By:
Clinical Genetics|June 26, 2002
Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigreesM Arcos-Burgos, F X Castellanos, F Lopera, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Revista De Neurologia|April 3, 2009
[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]N Trujillo-Orrego, D A Pineda, C P Arango, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Genes, Brain, and Behavior|November 3, 2010
Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication studyM Ribasés, J A Ramos-Quiroga, C Sánchez-Mora, et al.
American Journal of Human Genetics|October 10, 2007
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.
Molecular Psychiatry|November 25, 2015
Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolateC A Mastronardi, E Pillai, D A Pineda, et al.
Nature Genetics|November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Clinical Genetics|June 26, 2002
Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigreesM Arcos-Burgos, F X Castellanos, F Lopera, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Revista De Neurologia|April 3, 2009
[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]N Trujillo-Orrego, D A Pineda, C P Arango, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.
Genes, Brain, and Behavior|November 3, 2010
Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication studyM Ribasés, J A Ramos-Quiroga, C Sánchez-Mora, et al.
American Journal of Human Genetics|October 10, 2007
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humansJ D Karkera, J S Lee, E Roessler, et al.
Molecular Psychiatry|November 25, 2015
Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolateC A Mastronardi, E Pillai, D A Pineda, et al.
Nature Genetics|November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Pageof 11