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B T Teh

Showing results (71-80 of 128) with videos related to

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British Journal of Cancer|January 16, 2008
Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinomaM R Morris, D Gentle, M Abdulrahman, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Genotyping of adrenocortical tumors: very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16M Kjellman, L Roshani, B T Teh, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Clinical Endocrinology|July 9, 1999
Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndromeW S Wassif, F Farnebo, B T Teh, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|January 19, 2006
[Prophylactic parathyroidectomy for familial parathyroid carcinoma]O Gimm, K Lorenz, P Nguyen Thanh, et al.
American Journal of Human Genetics|October 30, 1998
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumorsB T Teh, C T Esapa, R Houlston, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34H Koillinen, F K Wong, J Rautio, et al.
Human Genetics|March 1, 1997
Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidismF Farnebo, B T Teh, C Dotzenrath, et al.
Journal of Medical Genetics|March 10, 2001
Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinomaH Kanayama, W O Lui, M Takahashi, et al.
Journal of Medical Genetics|May 19, 2001
Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndromeF K Wong, H Koillinen, J Rautio, et al.
Pageof 13

Showing results (71-80 of 128) with videos related to

Sort By:
Pageof 13
British Journal of Cancer|January 16, 2008
Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinomaM R Morris, D Gentle, M Abdulrahman, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Genotyping of adrenocortical tumors: very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16M Kjellman, L Roshani, B T Teh, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Clinical Endocrinology|July 9, 1999
Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndromeW S Wassif, F Farnebo, B T Teh, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|January 19, 2006
[Prophylactic parathyroidectomy for familial parathyroid carcinoma]O Gimm, K Lorenz, P Nguyen Thanh, et al.
American Journal of Human Genetics|October 30, 1998
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumorsB T Teh, C T Esapa, R Houlston, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34H Koillinen, F K Wong, J Rautio, et al.
Human Genetics|March 1, 1997
Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidismF Farnebo, B T Teh, C Dotzenrath, et al.
Journal of Medical Genetics|March 10, 2001
Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinomaH Kanayama, W O Lui, M Takahashi, et al.
Journal of Medical Genetics|May 19, 2001
Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndromeF K Wong, H Koillinen, J Rautio, et al.
Pageof 13