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

S Ellard

Showing results (81-90 of 144) with videos related to

Pageof 15
Sort By:
Diabetologia|November 13, 2008
Prevalence of GCK mutations in individuals screened for fasting hyperglycaemiaA L Gloyn, M van de Bunt, I M Stratton, et al.
American Journal of Human Genetics|June 12, 1999
A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3P D Turnpenny, M P Bulman, T M Frayling, et al.
Diabetes|July 2, 1998
Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.KF Beards, T Frayling, M Bulman, et al.
Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.
Clinical Genetics|June 18, 2004
Pseudodominant inheritance of spondylocostal dysostosis type 1 caused by two familial delta-like 3 mutationsN V Whittock, S Ellard, J Duncan, et al.
Diabetologia|July 10, 2007
Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunctionJ A L Minton, M van de Bunt, C Boustred, et al.
Pediatric Diabetes|March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotoniaS E Flanagan, F Vairo, M B Johnson, et al.
Diabetes|April 2, 1999
Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the youngS Ellard, M P Bulman, T M Frayling, et al.
Medical Oncology (Northwood, London, England)|April 1, 2003
Quantitation of cyclin D1 over-expression using competitive fluorescent reverse transcription polymerase chain reaction: a tool for the differential diagnosis of mantle cell lymphomaC L Wickham, H Armitage, M V Joyner, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2008
Severe intrauterine growth retardation and atypical diabetes associated with a translocation breakpoint disrupting regulation of the insulin-like growth factor 2 geneR Murphy, J Baptista, J Holly, et al.
Pageof 15

Showing results (81-90 of 144) with videos related to

Sort By:
Pageof 15
Diabetologia|November 13, 2008
Prevalence of GCK mutations in individuals screened for fasting hyperglycaemiaA L Gloyn, M van de Bunt, I M Stratton, et al.
American Journal of Human Genetics|June 12, 1999
A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3P D Turnpenny, M P Bulman, T M Frayling, et al.
Diabetes|July 2, 1998
Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.KF Beards, T Frayling, M Bulman, et al.
Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.
Clinical Genetics|June 18, 2004
Pseudodominant inheritance of spondylocostal dysostosis type 1 caused by two familial delta-like 3 mutationsN V Whittock, S Ellard, J Duncan, et al.
Diabetologia|July 10, 2007
Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunctionJ A L Minton, M van de Bunt, C Boustred, et al.
Pediatric Diabetes|March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotoniaS E Flanagan, F Vairo, M B Johnson, et al.
Diabetes|April 2, 1999
Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the youngS Ellard, M P Bulman, T M Frayling, et al.
Medical Oncology (Northwood, London, England)|April 1, 2003
Quantitation of cyclin D1 over-expression using competitive fluorescent reverse transcription polymerase chain reaction: a tool for the differential diagnosis of mantle cell lymphomaC L Wickham, H Armitage, M V Joyner, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2008
Severe intrauterine growth retardation and atypical diabetes associated with a translocation breakpoint disrupting regulation of the insulin-like growth factor 2 geneR Murphy, J Baptista, J Holly, et al.
Pageof 15