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

J D Brook

Showing results (61-70 of 72) with videos related to

Pageof 8
Sort By:
Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.
Cell|February 21, 1992
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family memberJ D Brook, M E McCurrach, H G Harley, et al.
Genomics|July 1, 1992
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19qG Jansen, P J de Jong, C Amemiya, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
Cell|April 17, 1992
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family memberJ D Brook, M E McCurrach, H G Harley, et al.
Genomics|June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locusJ D Brook, B V Zemelman, K Hadingham, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
American Journal of Human Genetics|November 1, 1995
Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversalC Kwok, P A Weller, S Guioli, et al.
American Journal of Human Genetics|December 1, 1996
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 geneJ A Terrett, R Newbury-Ecob, N M Smith, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.
Cell|February 21, 1992
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family memberJ D Brook, M E McCurrach, H G Harley, et al.
Genomics|July 1, 1992
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19qG Jansen, P J de Jong, C Amemiya, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
Cell|April 17, 1992
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family memberJ D Brook, M E McCurrach, H G Harley, et al.
Genomics|June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locusJ D Brook, B V Zemelman, K Hadingham, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
American Journal of Human Genetics|November 1, 1995
Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversalC Kwok, P A Weller, S Guioli, et al.
American Journal of Human Genetics|December 1, 1996
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 geneJ A Terrett, R Newbury-Ecob, N M Smith, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 8