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 D Weston

Showing results (11-20 of 39) with videos related to

Pageof 4
Sort By:
Human Genetics|April 6, 1999
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutationsS Usami, S Abe, M D Weston, et al.
Genomics|April 12, 2005
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IICK R Johnson, Q Y Zheng, M D Weston, et al.
Human Molecular Genetics|June 1, 1993
Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR)S P Dahl, M D Weston, L D Overbeck, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regionsS Pieke Dahl, M D Weston, W J Kimberling, et al.
Journal of Medical Genetics|October 1, 1993
Genetic heterogeneity of Usher syndrome type IIS Pieke Dahl, W J Kimberling, M B Gorin, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A progress report on the localization of Usher syndrome type II to chromosome 1qM D Weston, W J Kimberling, C G Möller, et al.
The British Journal of Surgery|March 2, 2002
Phase I study of percutaneous cryotherapy for colorectal liver metastasisA Huang, J M McCall, M D Weston, et al.
Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.
Human Mutation|September 30, 1999
Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.
Human Mutation|May 29, 1998
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndromeS Kumar, W J Kimberling, M D Weston, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Human Genetics|April 6, 1999
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutationsS Usami, S Abe, M D Weston, et al.
Genomics|April 12, 2005
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IICK R Johnson, Q Y Zheng, M D Weston, et al.
Human Molecular Genetics|June 1, 1993
Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR)S P Dahl, M D Weston, L D Overbeck, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regionsS Pieke Dahl, M D Weston, W J Kimberling, et al.
Journal of Medical Genetics|October 1, 1993
Genetic heterogeneity of Usher syndrome type IIS Pieke Dahl, W J Kimberling, M B Gorin, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A progress report on the localization of Usher syndrome type II to chromosome 1qM D Weston, W J Kimberling, C G Möller, et al.
The British Journal of Surgery|March 2, 2002
Phase I study of percutaneous cryotherapy for colorectal liver metastasisA Huang, J M McCall, M D Weston, et al.
Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.
Human Mutation|September 30, 1999
Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.
Human Mutation|May 29, 1998
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndromeS Kumar, W J Kimberling, M D Weston, et al.
Pageof 4