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

D H Ledbetter

Showing results (71-80 of 251) with videos related to

Pageof 26
Sort By:
American Journal of Medical Genetics|January 1, 1981
Phenotype associated with ring 10 chromosome: report of patient and review of literatureV V Michels, D J Driscoll, D H Ledbetter, et al.
Fertility and Sterility|December 1, 1985
A trisomic child after in vitro fertilization: result of paternal nondisjunctionJ F Hejtmancik, D H Ledbetter, A L Beaudet, et al.
Nucleic Acids Research|July 11, 1988
Cosmid 128 defines three RFLPs on chromosome 17q23-qter. [HGM9 no. D17S77]M Litt, S Kondoleon, H Vissing, et al.
Journal of Medical Genetics|January 1, 1996
Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisationH M Kingston, D H Ledbetter, P I Tomlin, et al.
Genome Research|October 6, 1999
Characterization of physical gap sizes at human telomeresC M Lese, J A Fantes, H C Riethman, et al.
Human Genetics|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.
American Journal of Medical Genetics|August 1, 1991
Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2)J R Lupski, C Langston, R Friedman, et al.
American Journal of Human Genetics|September 1, 1985
Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activityE S Cantú, R L Nussbaum, S D Airhart, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Localization of mouse phenylalanine hydroxylase locus on chromosome 10F D Ledley, S A Ledbetter, D H Ledbetter, et al.
American Journal of Medical Genetics|August 1, 1985
A new family with fra(10)(q25): spontaneous expression and 100% expression with 100 microM BrdUS M Gollin, H G Bock, C T Caskey, et al.
Pageof 26

Showing results (71-80 of 251) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics|January 1, 1981
Phenotype associated with ring 10 chromosome: report of patient and review of literatureV V Michels, D J Driscoll, D H Ledbetter, et al.
Fertility and Sterility|December 1, 1985
A trisomic child after in vitro fertilization: result of paternal nondisjunctionJ F Hejtmancik, D H Ledbetter, A L Beaudet, et al.
Nucleic Acids Research|July 11, 1988
Cosmid 128 defines three RFLPs on chromosome 17q23-qter. [HGM9 no. D17S77]M Litt, S Kondoleon, H Vissing, et al.
Journal of Medical Genetics|January 1, 1996
Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisationH M Kingston, D H Ledbetter, P I Tomlin, et al.
Genome Research|October 6, 1999
Characterization of physical gap sizes at human telomeresC M Lese, J A Fantes, H C Riethman, et al.
Human Genetics|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.
American Journal of Medical Genetics|August 1, 1991
Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2)J R Lupski, C Langston, R Friedman, et al.
American Journal of Human Genetics|September 1, 1985
Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activityE S Cantú, R L Nussbaum, S D Airhart, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Localization of mouse phenylalanine hydroxylase locus on chromosome 10F D Ledley, S A Ledbetter, D H Ledbetter, et al.
American Journal of Medical Genetics|August 1, 1985
A new family with fra(10)(q25): spontaneous expression and 100% expression with 100 microM BrdUS M Gollin, H G Bock, C T Caskey, et al.
Pageof 26