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

C G Mathew

Showing results (21-30 of 129) with videos related to

Pageof 13
Sort By:
Lancet (London, England)|January 30, 1993
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophyS C Yau, R G Roberts, M Bobrow, et al.
British Journal of Haematology|September 1, 1983
The molecular basis of alpha thalassaemia in a South African populationC G Mathew, J Rousseau, J S Rees, et al.
Lancet (London, England)|January 5, 1991
Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative GroupC G Mathew, D F Easton, Y Nakamura, et al.
Journal of Medical Genetics|July 1, 1996
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysisS C Yau, M Bobrow, C G Mathew, et al.
Human Molecular Genetics|January 1, 1993
Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCRR A Gibson, M Buchwald, R G Roberts, et al.
FEBS Letters|March 9, 1981
The protein composition of rat satellite chromatinC G Mathew, G H Goodwin, T Igo-Kemenes, et al.
Genetic Testing|January 1, 1997
Dystrophin point mutation screening using a multiplexed protein truncation testN V Whittock, R G Roberts, C G Mathew, et al.
Cell Biology International Reports|January 1, 1981
The high mobility group proteins and transcribed nucleosomesC G Mathew, G H Goodwin, C A Wright, et al.
Journal of Medical Genetics|May 1, 1991
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methodsS Abbs, S C Yau, S Clark, et al.
Human Molecular Genetics|June 1, 1993
A nonsense mutation and exon skipping in the Fanconi anaemia group C geneR A Gibson, A Hajianpour, M Murer-Orlando, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|January 30, 1993
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophyS C Yau, R G Roberts, M Bobrow, et al.
British Journal of Haematology|September 1, 1983
The molecular basis of alpha thalassaemia in a South African populationC G Mathew, J Rousseau, J S Rees, et al.
Lancet (London, England)|January 5, 1991
Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative GroupC G Mathew, D F Easton, Y Nakamura, et al.
Journal of Medical Genetics|July 1, 1996
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysisS C Yau, M Bobrow, C G Mathew, et al.
Human Molecular Genetics|January 1, 1993
Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCRR A Gibson, M Buchwald, R G Roberts, et al.
FEBS Letters|March 9, 1981
The protein composition of rat satellite chromatinC G Mathew, G H Goodwin, T Igo-Kemenes, et al.
Genetic Testing|January 1, 1997
Dystrophin point mutation screening using a multiplexed protein truncation testN V Whittock, R G Roberts, C G Mathew, et al.
Cell Biology International Reports|January 1, 1981
The high mobility group proteins and transcribed nucleosomesC G Mathew, G H Goodwin, C A Wright, et al.
Journal of Medical Genetics|May 1, 1991
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methodsS Abbs, S C Yau, S Clark, et al.
Human Molecular Genetics|June 1, 1993
A nonsense mutation and exon skipping in the Fanconi anaemia group C geneR A Gibson, A Hajianpour, M Murer-Orlando, et al.
Pageof 13