R M Hofstra - JoVE Visualize

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Cancer Research|March 15, 1992

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancerB Carritt, K Kok, A van den Berg, et al.

The Journal of Investigative Dermatology|August 1, 1996

RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasiaR M Hofstra, R H Sijmons, T Stelwagen, et al.

Human Genetics|May 26, 1998

Three novel KCNA1 mutations in episodic ataxia type I familiesH Scheffer, E R Brunt, G J Mol, et al.

American Journal of Human Genetics|October 16, 1999

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutationsY Wu, M J Berends, R G Mensink, et al.

Human Molecular Genetics|June 1, 1996

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancerM Nyström-Lahti, Y Wu, A L Moisio, et al.

American Journal of Medical Genetics|August 17, 1999

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22J B Verheij, K Bouman, R A van Lingen, et al.

Nature Genetics|April 1, 1996

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)R M Hofstra, J Osinga, G Tan-Sindhunata, et al.

Neurogenetics|November 21, 2001

Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysisM Boon, I M Nolte, M Bruinenberg, et al.

Gut|November 21, 1998

Oncological implications of RET gene mutations in Hirschsprung's diseaseR H Sijmons, R M Hofstra, F A Wijburg, et al.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1996

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of casesR M Hofstra, T Stelwagen, R P Stulp, et al.

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Showing results (41-50 of 56) with videos related to

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Pageof 6

Cancer Research|March 15, 1992

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancerB Carritt, K Kok, A van den Berg, et al.

The Journal of Investigative Dermatology|August 1, 1996

RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasiaR M Hofstra, R H Sijmons, T Stelwagen, et al.

Human Genetics|May 26, 1998

Three novel KCNA1 mutations in episodic ataxia type I familiesH Scheffer, E R Brunt, G J Mol, et al.

American Journal of Human Genetics|October 16, 1999

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutationsY Wu, M J Berends, R G Mensink, et al.

Human Molecular Genetics|June 1, 1996

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancerM Nyström-Lahti, Y Wu, A L Moisio, et al.

American Journal of Medical Genetics|August 17, 1999

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22J B Verheij, K Bouman, R A van Lingen, et al.

Nature Genetics|April 1, 1996

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)R M Hofstra, J Osinga, G Tan-Sindhunata, et al.

Neurogenetics|November 21, 2001

Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysisM Boon, I M Nolte, M Bruinenberg, et al.

Gut|November 21, 1998

Oncological implications of RET gene mutations in Hirschsprung's diseaseR H Sijmons, R M Hofstra, F A Wijburg, et al.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1996

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of casesR M Hofstra, T Stelwagen, R P Stulp, et al.

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