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 Willems

Showing results (391-400 of 446) with videos related to

Pageof 45
Sort By:
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach-Rott syndromeVered Shkalim, Hagit N Baris, Gavriel Gal, et al.
Lancet (London, England)|March 27, 2001
Variant esp gene as a marker of a distinct genetic lineage of vancomycin-resistant Enterococcus faecium spreading in hospitalsR J Willems, W Homan, J Top, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Annals of the Rheumatic Diseases|December 16, 2003
Satisfactory cross cultural equivalence of the Dutch WOMAC in patients with hip osteoarthritis waiting for arthroplastyL D Roorda, C A Jones, M Waltz, et al.
American Journal of Medical Genetics|February 27, 2001
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examinationS A Irwin, B Patel, M Idupulapati, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Pageof 45

Showing results (391-400 of 446) with videos related to

Sort By:
Pageof 45
Journal of Medical Genetics|June 30, 2000
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndromeP J Coucke, P Van Hauwe, L A Everett, et al.
American Journal of Medical Genetics. Part A|November 19, 2009
Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach-Rott syndromeVered Shkalim, Hagit N Baris, Gavriel Gal, et al.
Lancet (London, England)|March 27, 2001
Variant esp gene as a marker of a distinct genetic lineage of vancomycin-resistant Enterococcus faecium spreading in hospitalsR J Willems, W Homan, J Top, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Annals of the Rheumatic Diseases|December 16, 2003
Satisfactory cross cultural equivalence of the Dutch WOMAC in patients with hip osteoarthritis waiting for arthroplastyL D Roorda, C A Jones, M Waltz, et al.
American Journal of Medical Genetics|February 27, 2001
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examinationS A Irwin, B Patel, M Idupulapati, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
American Journal of Human Genetics|January 13, 2000
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)E Holinski-Feder, E Reyniers, S Uhrig, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Pageof 45