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Showing results (241-250 of 263) with videos related to

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Human Genetics|August 1, 1993
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH)M E Phipps, E R Maher, N A Affara, et al.
Human Genetics|September 1, 1996
Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central EuropeD Glavac, H P Neumann, C Wittke, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Cancer Research|May 1, 1998
Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogeneL Schmidt, K Junker, G Weirich, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
AJR. American Journal of Roentgenology|December 1, 1992
The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patientsP L Choyke, G M Glenn, M M Walther, et al.
The Journal of Urology|August 24, 1999
Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytomaM M Walther, R Reiter, H R Keiser, et al.
Surgery|December 15, 2000
Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau diseaseS K Libutti, P L Choyke, H R Alexander, et al.
American Journal of Epidemiology|May 1, 1970
Serologic surveys of human cancer patients for antibody to adenovirus T antigensR V Gilden, J Kern, Y K Lee, et al.
Nature Genetics|September 10, 1998
Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomasZ Zhuang, W S Park, S Pack, et al.
Pageof 27

Showing results (241-250 of 263) with videos related to

Sort By:
Pageof 27
Human Genetics|August 1, 1993
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH)M E Phipps, E R Maher, N A Affara, et al.
Human Genetics|September 1, 1996
Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central EuropeD Glavac, H P Neumann, C Wittke, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Cancer Research|May 1, 1998
Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogeneL Schmidt, K Junker, G Weirich, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
AJR. American Journal of Roentgenology|December 1, 1992
The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patientsP L Choyke, G M Glenn, M M Walther, et al.
The Journal of Urology|August 24, 1999
Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytomaM M Walther, R Reiter, H R Keiser, et al.
Surgery|December 15, 2000
Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau diseaseS K Libutti, P L Choyke, H R Alexander, et al.
American Journal of Epidemiology|May 1, 1970
Serologic surveys of human cancer patients for antibody to adenovirus T antigensR V Gilden, J Kern, Y K Lee, et al.
Nature Genetics|September 10, 1998
Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomasZ Zhuang, W S Park, S Pack, et al.
Pageof 27