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

H G Harley

Showing results (1-10 of 35) with videos related to

Pageof 4
Sort By:
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.
Human Genetics|August 1, 1989
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sitesD J Shaw, H G Harley, J D Brook, et al.
Nucleic Acids Research|February 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Human Molecular Genetics|September 1, 1992
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeatS R Crow, H G Harley, J D Brook, et al.
Journal of Medical Genetics|September 1, 1995
Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophyJ Poulton, H G Harley, J Dasmahapatra, et al.
Nucleic Acids Research|August 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Nucleic Acids Research|February 25, 1990
A polymorphic DNA clone which maps to 19q13.2-19qter (D19S62)J D Brook, K V Walsh, H G Harley, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.
Journal of Medical Genetics|February 1, 1986
Gene mapping and chromosome 19D J Shaw, J D Brook, A L Meredith, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.
Human Genetics|August 1, 1989
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sitesD J Shaw, H G Harley, J D Brook, et al.
Nucleic Acids Research|February 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Human Molecular Genetics|September 1, 1992
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeatS R Crow, H G Harley, J D Brook, et al.
Journal of Medical Genetics|September 1, 1995
Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophyJ Poulton, H G Harley, J Dasmahapatra, et al.
Nucleic Acids Research|August 25, 1990
RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63)J D Brook, H G Harley, S A Rundle, et al.
Nucleic Acids Research|February 25, 1990
A polymorphic DNA clone which maps to 19q13.2-19qter (D19S62)J D Brook, K V Walsh, H G Harley, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.
Journal of Medical Genetics|February 1, 1986
Gene mapping and chromosome 19D J Shaw, J D Brook, A L Meredith, et al.
Pageof 4