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

M Bobrow

Showing results (191-200 of 235) with videos related to

Pageof 24
Sort By:
Clinical Genetics|April 1, 1989
Molecular deletions in the Duchenne/Becker muscular dystrophy geneK A Hart, S Abbs, M C Wapenaar, et al.
Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Birth Defects Original Article Series|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
British Journal of Cancer|August 19, 2007
The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary careJ Emery, H Morris, R Goodchild, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Counselling following diagnosis of fetal abnormality: a comparison between German, Portuguese and UK geneticistsT Marteau, H Drake, M Reid, et al.
Lancet (London, England)|April 19, 1986
DNA deletion in boy with Becker muscular dystrophyS Hodgson, K Hart, A Walker, et al.
Somatic Cell Genetics|March 1, 1976
Human gene mapping using an X/autosome translocationE Solomon, M Bobrow, P N Goodfellow, et al.
Prenatal Diagnosis|November 1, 1985
A survey of diagnostic amniocenteses in Oxford from 1974-1981E Terzian, J Boreham, H S Cuckle, et al.
Journal of Molecular Biology|July 25, 1997
Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouseA K Dixon, T M Tait, E A Campbell, et al.
Pageof 24

Showing results (191-200 of 235) with videos related to

Sort By:
Pageof 24
Clinical Genetics|April 1, 1989
Molecular deletions in the Duchenne/Becker muscular dystrophy geneK A Hart, S Abbs, M C Wapenaar, et al.
Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.
Birth Defects Original Article Series|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
British Journal of Cancer|August 19, 2007
The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary careJ Emery, H Morris, R Goodchild, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Counselling following diagnosis of fetal abnormality: a comparison between German, Portuguese and UK geneticistsT Marteau, H Drake, M Reid, et al.
Lancet (London, England)|April 19, 1986
DNA deletion in boy with Becker muscular dystrophyS Hodgson, K Hart, A Walker, et al.
Somatic Cell Genetics|March 1, 1976
Human gene mapping using an X/autosome translocationE Solomon, M Bobrow, P N Goodfellow, et al.
Prenatal Diagnosis|November 1, 1985
A survey of diagnostic amniocenteses in Oxford from 1974-1981E Terzian, J Boreham, H S Cuckle, et al.
Journal of Molecular Biology|July 25, 1997
Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouseA K Dixon, T M Tait, E A Campbell, et al.
Pageof 24