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P K Rogan

Showing results (31-40 of 45) with videos related to

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American Journal of Medical Genetics|March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromesP K Rogan, J R Seip, D J Driscoll, et al.
Human Genetics|January 28, 1999
Relaxation of imprinting in Prader-Willi syndromeP K Rogan, J R Seip, L M White, et al.
American Journal of Medical Genetics|September 20, 1996
Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndromeA N Vgontzas, A Kales, J Seip, et al.
Current Oncology (Toronto, Ont.)|November 2, 2017
The clinical significance of occult gynecologic primary tumours in metastatic cancerM B Hannouf, E Winquist, S M Mahmud, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutationsS Saitoh, K Buiting, P K Rogan, et al.
Current Oncology (Toronto, Ont.)|November 23, 2018
Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in OntarioC S Kim, M B Hannouf, S Sarma, et al.
Genomics|November 20, 1995
Microsatellite-centromere mapping in the zebrafish (Danio rerio)E J Kauffman, E E Gestl, D J Kim, et al.
The Pharmacogenomics Journal|March 16, 2005
Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African AmericansA Gaedigk, A Bhathena, L Ndjountché, 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 1, 1994
Bloom syndrome and maternal uniparental disomy for chromosome 15T Woodage, M Prasad, J W Dixon, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromesP K Rogan, J R Seip, D J Driscoll, et al.
Human Genetics|January 28, 1999
Relaxation of imprinting in Prader-Willi syndromeP K Rogan, J R Seip, L M White, et al.
American Journal of Medical Genetics|September 20, 1996
Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndromeA N Vgontzas, A Kales, J Seip, et al.
Current Oncology (Toronto, Ont.)|November 2, 2017
The clinical significance of occult gynecologic primary tumours in metastatic cancerM B Hannouf, E Winquist, S M Mahmud, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutationsS Saitoh, K Buiting, P K Rogan, et al.
Current Oncology (Toronto, Ont.)|November 23, 2018
Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in OntarioC S Kim, M B Hannouf, S Sarma, et al.
Genomics|November 20, 1995
Microsatellite-centromere mapping in the zebrafish (Danio rerio)E J Kauffman, E E Gestl, D J Kim, et al.
The Pharmacogenomics Journal|March 16, 2005
Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African AmericansA Gaedigk, A Bhathena, L Ndjountché, 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 1, 1994
Bloom syndrome and maternal uniparental disomy for chromosome 15T Woodage, M Prasad, J W Dixon, et al.
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