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

G Norbury

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Clinical Genetics|October 22, 2009
Mutation screening in patients for familial hypercholesterolaemia (ADH)A Taylor, K Patel, J Tsedeke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2004
Homozygous hypercholesterolaemia and ezetimibe: a case reportC J Hendriksz, G Norbury, S Tabrah, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 14, 1980
Flunitrazepam for the intravenous induction of anaesthesia in childrenJ G Brock-Utne, A G Norbury, A M Holloway, et al.
Clinical Genetics|June 23, 2009
Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemiaA Taylor, B Martin, D Wang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Incorrect diagnosis of myotonic dystrophy and its potential consequences revealed by subsequent direct genetic analysisP R Barnes, D Hilton-Jones, G Norbury, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Journal of the Neurological Sciences|May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'S M White, S S Gubbay, C G Norbury, et al.
Applied Health Economics and Health Policy|April 21, 2015
Cost Effectiveness of Using Array-CGH for Diagnosing Learning DisabilityG S Sagoo, S Mohammed, G Barton, et al.
Fetal Diagnosis and Therapy|December 17, 2008
Apert syndrome: the current role of prenatal ultrasound and genetic analysis in diagnosis and counsellingA P Athanasiadis, M Zafrakas, P Polychronou, et al.
Neurology|September 26, 1997
Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Clinical Genetics|October 22, 2009
Mutation screening in patients for familial hypercholesterolaemia (ADH)A Taylor, K Patel, J Tsedeke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2004
Homozygous hypercholesterolaemia and ezetimibe: a case reportC J Hendriksz, G Norbury, S Tabrah, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 14, 1980
Flunitrazepam for the intravenous induction of anaesthesia in childrenJ G Brock-Utne, A G Norbury, A M Holloway, et al.
Clinical Genetics|June 23, 2009
Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemiaA Taylor, B Martin, D Wang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Incorrect diagnosis of myotonic dystrophy and its potential consequences revealed by subsequent direct genetic analysisP R Barnes, D Hilton-Jones, G Norbury, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Journal of the Neurological Sciences|May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'S M White, S S Gubbay, C G Norbury, et al.
Applied Health Economics and Health Policy|April 21, 2015
Cost Effectiveness of Using Array-CGH for Diagnosing Learning DisabilityG S Sagoo, S Mohammed, G Barton, et al.
Fetal Diagnosis and Therapy|December 17, 2008
Apert syndrome: the current role of prenatal ultrasound and genetic analysis in diagnosis and counsellingA P Athanasiadis, M Zafrakas, P Polychronou, et al.
Neurology|September 26, 1997
Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Pageof 3