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

R Weksberg

Showing results (11-20 of 84) with videos related to

Pageof 9
Sort By:
Nature Genetics|March 1, 1996
Glypicans: a growing trendR Weksberg, J A Squire, D M Templeton
Human Mutation|January 1, 1997
Example of somatic mosaicism in a series of de novo neurofibromatosis type 1 cases due to a maternally derived deletionP J Ainsworth, P K Chakraborty, R Weksberg
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|January 30, 2002
Music skills and the expressive interpretation of music in children with Williams-Beuren syndrome: pitch, rhythm, melodic imagery, phrasing, and musical affectT Hopyan, M Dennis, R Weksberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Structural alterations of DNA ligase I in Bloom syndromeA E Willis, R Weksberg, S Tomlinson, et al.
Clinical Genetics|December 1, 1996
Abnormal extracellular matrix in Ehlers-Danlos syndrome type IV due to the substitution of glycine 934 by glutamic acid in the triple helical domain of type III collagenJ McGrory, R Weksberg, P Thorner, et al.
American Journal of Human Genetics|June 1, 1988
Bloom syndrome: a single complementation group defines patients of diverse ethnic originR Weksberg, C Smith, L Anson-Cartwright, et al.
American Journal of Human Genetics|October 1, 1996
Parental attitudes to genetic counseling and predictive testing for childhood cancerD Malkin, K Australie, C Shuman, et al.
American Journal of Medical Genetics|May 8, 1999
Cardiac anomalies in the Simpson-Golabi-Behmel syndromeA E Lin, G Neri, R Hughes-Benzie, et al.
American Journal of Medical Genetics|September 24, 1999
Phenotype of adults with the 22q11 deletion syndrome: A reviewE Cohen, E W Chow, R Weksberg, et al.
American Journal of Human Genetics|August 12, 1999
Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndromeL M Brzustowicz, S Farrell, M B Khan, et al.
Pageof 9

Showing results (11-20 of 84) with videos related to

Sort By:
Pageof 9
Nature Genetics|March 1, 1996
Glypicans: a growing trendR Weksberg, J A Squire, D M Templeton
Human Mutation|January 1, 1997
Example of somatic mosaicism in a series of de novo neurofibromatosis type 1 cases due to a maternally derived deletionP J Ainsworth, P K Chakraborty, R Weksberg
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|January 30, 2002
Music skills and the expressive interpretation of music in children with Williams-Beuren syndrome: pitch, rhythm, melodic imagery, phrasing, and musical affectT Hopyan, M Dennis, R Weksberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Structural alterations of DNA ligase I in Bloom syndromeA E Willis, R Weksberg, S Tomlinson, et al.
Clinical Genetics|December 1, 1996
Abnormal extracellular matrix in Ehlers-Danlos syndrome type IV due to the substitution of glycine 934 by glutamic acid in the triple helical domain of type III collagenJ McGrory, R Weksberg, P Thorner, et al.
American Journal of Human Genetics|June 1, 1988
Bloom syndrome: a single complementation group defines patients of diverse ethnic originR Weksberg, C Smith, L Anson-Cartwright, et al.
American Journal of Human Genetics|October 1, 1996
Parental attitudes to genetic counseling and predictive testing for childhood cancerD Malkin, K Australie, C Shuman, et al.
American Journal of Medical Genetics|May 8, 1999
Cardiac anomalies in the Simpson-Golabi-Behmel syndromeA E Lin, G Neri, R Hughes-Benzie, et al.
American Journal of Medical Genetics|September 24, 1999
Phenotype of adults with the 22q11 deletion syndrome: A reviewE Cohen, E W Chow, R Weksberg, et al.
American Journal of Human Genetics|August 12, 1999
Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndromeL M Brzustowicz, S Farrell, M B Khan, et al.
Pageof 9