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 Goodship

Showing results (31-40 of 137) with videos related to

Pageof 14
Sort By:
Prenatal Diagnosis|August 1, 1995
A case of paternal uniparental disomy for chromosome 11A Webb, J Beard, C Wright, et al.
British Journal of Haematology|October 14, 2009
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United KingdomC Mark Taylor, Sam Machin, Stephen J Wigmore, et al.
Prenatal Diagnosis|October 8, 1997
Renal abnormalities on obstetric ultrasound as a presentation of DiGeorge syndromeJ Goodship, S C Robson, S Sturgiss, et al.
Immunobiology|September 9, 2011
Complement polymorphisms: geographical distribution and relevance to diseaseL Ermini, I J Wilson, T H J Goodship, et al.
Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Blood|June 15, 1991
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probeJ Goodship, J Carter, T Espanol, et al.
Human Mutation|November 11, 2005
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutationsRebecca E Saunders, Timothy H J Goodship, Peter F Zipfel, et al.
Nephron Extra|October 29, 2013
Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest EnglandAlexander J Hamilton, Carl B A Lyons, Timothy H J Goodship, et al.
American Journal of Human Genetics|July 1, 1994
A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individualsD Bourn, S A Carter, D G Evans, et al.
Human Genetics|March 1, 1994
Mutation screening by a combination of biotin-SSCP and direct sequencingA S Virdi, J A Loughlin, C M Irven, et al.
Pageof 14

Showing results (31-40 of 137) with videos related to

Sort By:
Pageof 14
Prenatal Diagnosis|August 1, 1995
A case of paternal uniparental disomy for chromosome 11A Webb, J Beard, C Wright, et al.
British Journal of Haematology|October 14, 2009
Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United KingdomC Mark Taylor, Sam Machin, Stephen J Wigmore, et al.
Prenatal Diagnosis|October 8, 1997
Renal abnormalities on obstetric ultrasound as a presentation of DiGeorge syndromeJ Goodship, S C Robson, S Sturgiss, et al.
Immunobiology|September 9, 2011
Complement polymorphisms: geographical distribution and relevance to diseaseL Ermini, I J Wilson, T H J Goodship, et al.
Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Blood|June 15, 1991
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probeJ Goodship, J Carter, T Espanol, et al.
Human Mutation|November 11, 2005
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutationsRebecca E Saunders, Timothy H J Goodship, Peter F Zipfel, et al.
Nephron Extra|October 29, 2013
Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest EnglandAlexander J Hamilton, Carl B A Lyons, Timothy H J Goodship, et al.
American Journal of Human Genetics|July 1, 1994
A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individualsD Bourn, S A Carter, D G Evans, et al.
Human Genetics|March 1, 1994
Mutation screening by a combination of biotin-SSCP and direct sequencingA S Virdi, J A Loughlin, C M Irven, et al.
Pageof 14