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 (151-160 of 235) with videos related to

Pageof 24
Sort By:
Cytogenetics and Cell Genetics|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, 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.
Cytogenetics|January 1, 1971
Length variation in the quinacrine-binding segment of human Y chromosomes of different sizesM Bobrow, P L Pearson, M C Pike, et al.
Journal of Medical Genetics|May 1, 1989
Fertility in a male with trisomy 21R Sheridan, J Llerena, S Matkins, et al.
Human Genetics|January 1, 1985
Two cases of X/autosome translocation in females with incontinentia pigmentiS V Hodgson, B Neville, R W Jones, et al.
Biochemical Genetics|October 1, 1980
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.)E Tolley, V van Heyningen, R Brown, et al.
Journal of Medical Genetics|April 3, 2004
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domainC Mattocks, D Baralle, P Tarpey, et al.
American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.
Human Molecular Genetics|January 1, 1993
Point mutation in a Becker muscular dystrophy patientR G Roberts, M R Passos-Bueno, M Bobrow, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Pageof 24

Showing results (151-160 of 235) with videos related to

Sort By:
Pageof 24
Cytogenetics and Cell Genetics|January 1, 1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybridsD A Hopkinson, S Povey, E Solomon, 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.
Cytogenetics|January 1, 1971
Length variation in the quinacrine-binding segment of human Y chromosomes of different sizesM Bobrow, P L Pearson, M C Pike, et al.
Journal of Medical Genetics|May 1, 1989
Fertility in a male with trisomy 21R Sheridan, J Llerena, S Matkins, et al.
Human Genetics|January 1, 1985
Two cases of X/autosome translocation in females with incontinentia pigmentiS V Hodgson, B Neville, R W Jones, et al.
Biochemical Genetics|October 1, 1980
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.)E Tolley, V van Heyningen, R Brown, et al.
Journal of Medical Genetics|April 3, 2004
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domainC Mattocks, D Baralle, P Tarpey, et al.
American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.
Human Molecular Genetics|January 1, 1993
Point mutation in a Becker muscular dystrophy patientR G Roberts, M R Passos-Bueno, M Bobrow, et al.
Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.
Pageof 24