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R D Nicholls

Showing results (91-100 of 107) with videos related to

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American Journal of Human Genetics|September 26, 2003
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsJ-H Chai, D P Locke, J M Greally, et al.
American Journal of Medical Genetics|May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndromeR D Nicholls, J H Knoll, K Glatt, et al.
Genomics|June 14, 2000
The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous systemT A Gray, L Hernandez, A H Carey, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
The New England Journal of Medicine|June 11, 1992
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosisM J Mascari, W Gottlieb, P K Rogan, et al.
American Journal of Human Genetics|July 27, 1999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpointsJ M Amos-Landgraf, Y Ji, W Gottlieb, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locusD R Higgs, J S Wainscoat, J Flint, et al.
Human Molecular Genetics|April 10, 1999
Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic regionM T Jong, A H Carey, K A Caldwell, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
American Journal of Medical Genetics|April 1, 1993
Cytogenetic and molecular analysis in Angelman syndromeJ L Zackowski, R D Nicholls, B A Gray, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|September 26, 2003
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsJ-H Chai, D P Locke, J M Greally, et al.
American Journal of Medical Genetics|May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndromeR D Nicholls, J H Knoll, K Glatt, et al.
Genomics|June 14, 2000
The ancient source of a distinct gene family encoding proteins featuring RING and C(3)H zinc-finger motifs with abundant expression in developing brain and nervous systemT A Gray, L Hernandez, A H Carey, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
The New England Journal of Medicine|June 11, 1992
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosisM J Mascari, W Gottlieb, P K Rogan, et al.
American Journal of Human Genetics|July 27, 1999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpointsJ M Amos-Landgraf, Y Ji, W Gottlieb, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locusD R Higgs, J S Wainscoat, J Flint, et al.
Human Molecular Genetics|April 10, 1999
Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic regionM T Jong, A H Carey, K A Caldwell, et al.
American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.
American Journal of Medical Genetics|April 1, 1993
Cytogenetic and molecular analysis in Angelman syndromeJ L Zackowski, R D Nicholls, B A Gray, et al.
Pageof 11