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R D Nicholls

Showing results (101-110 of 107) with videos related to

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Journal of Medical Genetics|December 19, 2001
Distinct phenotypes distinguish the molecular classes of Angelman syndromeA C Lossie, M M Whitney, D Amidon, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
Journal of Medical Genetics|December 19, 2001
Distinct phenotypes distinguish the molecular classes of Angelman syndromeA C Lossie, M M Whitney, D Amidon, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 11