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

P S Harper

Showing results (151-160 of 345) with videos related to

Pageof 35
Sort By:
Gene Therapy|January 1, 1994
Clinical considerations in gene therapy of Huntington's diseaseJ C MacMillan, R G Snell, P S Harper
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counsellingS M Huson, D A Compston, P S Harper
Journal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.
Journal of Medical Genetics|November 1, 1996
Huntington's disease predictive testing: the case for an assessment approach to requests from adolescentsJ Binedell, J R Soldan, J Scourfield, et al.
The Quarterly Journal of Medicine|July 1, 1970
Carcinoma of the oesophagus with tylosisP S Harper, R M Harper, A W Howel-Evans
Archives of Disease in Childhood|October 1, 1987
Clinical aspects of X-linked hypohidrotic ectodermal dysplasiaA Clarke, D I Phillips, R Brown, et al.
Journal of Medical Genetics|May 1, 1989
Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long armS H Roberts, M Upadhyaya, M Sarfarazi, et al.
Journal of Medical Genetics|March 1, 1988
Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)O W Quarrell, S Youngman, M Sarfarazi, et al.
Clinical Genetics|November 1, 1986
The problem of isolated cases of Huntington's disease in South Wales 1974-1984O W Quarrell, A Tyler, G Cole, et al.
American Journal of Medical Genetics|December 1, 1987
An integrated microcomputer system to maintain a genetic register for Huntington diseaseM Sarfarazi, O W Quarrell, G Wolak, et al.
Pageof 35

Showing results (151-160 of 345) with videos related to

Sort By:
Pageof 35
Gene Therapy|January 1, 1994
Clinical considerations in gene therapy of Huntington's diseaseJ C MacMillan, R G Snell, P S Harper
Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counsellingS M Huson, D A Compston, P S Harper
Journal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.
Journal of Medical Genetics|November 1, 1996
Huntington's disease predictive testing: the case for an assessment approach to requests from adolescentsJ Binedell, J R Soldan, J Scourfield, et al.
The Quarterly Journal of Medicine|July 1, 1970
Carcinoma of the oesophagus with tylosisP S Harper, R M Harper, A W Howel-Evans
Archives of Disease in Childhood|October 1, 1987
Clinical aspects of X-linked hypohidrotic ectodermal dysplasiaA Clarke, D I Phillips, R Brown, et al.
Journal of Medical Genetics|May 1, 1989
Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long armS H Roberts, M Upadhyaya, M Sarfarazi, et al.
Journal of Medical Genetics|March 1, 1988
Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)O W Quarrell, S Youngman, M Sarfarazi, et al.
Clinical Genetics|November 1, 1986
The problem of isolated cases of Huntington's disease in South Wales 1974-1984O W Quarrell, A Tyler, G Cole, et al.
American Journal of Medical Genetics|December 1, 1987
An integrated microcomputer system to maintain a genetic register for Huntington diseaseM Sarfarazi, O W Quarrell, G Wolak, et al.
Pageof 35