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

R D Nicholls

Showing results (71-80 of 107) with videos related to

Pageof 11
Sort By:
Journal of Medical Genetics|May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13W P Robinson, F Dutly, R D Nicholls, et al.
Molecular Biology and Evolution|October 19, 2001
The gene orders on human chromosome 15 and chicken chromosome 10 reveal multiple inter- and intrachromosomal rearrangementsR P Crooijmans, R J Dijkhof, T Veenendaal, et al.
Nucleic Acids Research|November 11, 1999
Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN lociT A Gray, M J Smithwick, M A Schaldach, et al.
Gene|December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25A Polvi, E Armstrong, C Lai, et al.
Genomics|August 1, 1992
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromesD J Driscoll, M F Waters, C A Williams, et al.
American Journal of Medical Genetics|April 1, 1993
Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structureC M Leonard, C A Williams, R D Nicholls, et al.
American Journal of Medical Genetics|June 13, 1997
Unexpected familial recurrence in Angelman syndromeK J Connerton-Moyer, R D Nicholls, S Schwartz, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 1999
Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 miceM Walkowicz, Y Ji, X Ren, et al.
British Medical Journal (Clinical Research Ed.)|May 4, 1985
Alpha thalassaemia in British peopleD R Higgs, H Ayyub, J B Clegg, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13W P Robinson, F Dutly, R D Nicholls, et al.
Molecular Biology and Evolution|October 19, 2001
The gene orders on human chromosome 15 and chicken chromosome 10 reveal multiple inter- and intrachromosomal rearrangementsR P Crooijmans, R J Dijkhof, T Veenendaal, et al.
Nucleic Acids Research|November 11, 1999
Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN lociT A Gray, M J Smithwick, M A Schaldach, et al.
Gene|December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25A Polvi, E Armstrong, C Lai, et al.
Genomics|August 1, 1992
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromesD J Driscoll, M F Waters, C A Williams, et al.
American Journal of Medical Genetics|April 1, 1993
Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structureC M Leonard, C A Williams, R D Nicholls, et al.
American Journal of Medical Genetics|June 13, 1997
Unexpected familial recurrence in Angelman syndromeK J Connerton-Moyer, R D Nicholls, S Schwartz, et al.
American Journal of Medical Genetics|October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndromeJ Clayton-Smith, D J Driscoll, M F Waters, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 1999
Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 miceM Walkowicz, Y Ji, X Ren, et al.
British Medical Journal (Clinical Research Ed.)|May 4, 1985
Alpha thalassaemia in British peopleD R Higgs, H Ayyub, J B Clegg, et al.
Pageof 11