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H P Neumann

Showing results (101-110 of 112) with videos related to

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Human Molecular Genetics|September 1, 1997
An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detectionT J Watnick, K B Piontek, T M Cordal, et al.
Genes, Chromosomes & Cancer|March 1, 1995
Mutation of the RET protooncogene in sporadic medullary thyroid carcinomaC Eng, L M Mulligan, D P Smith, et al.
Contributions to Nephrology|January 1, 1997
The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical managementH P Neumann, B U Bender, W Schultze-Seemann, et al.
American Journal of Human Genetics|December 1, 1994
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinomaJ M Whaley, J Naglich, L Gelbert, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, 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.
Journal of Medical Genetics|August 3, 2001
VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortalityB U Bender, C Eng, M Olschewski, et al.
Journal of the American Society of Nephrology : JASN|May 1, 1996
Identification of 17 mutations in ten exons in the COL4A5 collagen gene, but no mutations found in four exons in COL4A6: a study of 250 patients with hematuria and suspected of having Alport syndromeN Heiskari, X Zhang, J Zhou, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumorsD J Marsh, Z Zheng, A Arnold, et al.
Oncogene|May 18, 1999
Novel mutations of the MET proto-oncogene in papillary renal carcinomasL Schmidt, K Junker, N Nakaigawa, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|September 1, 1997
An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detectionT J Watnick, K B Piontek, T M Cordal, et al.
Genes, Chromosomes & Cancer|March 1, 1995
Mutation of the RET protooncogene in sporadic medullary thyroid carcinomaC Eng, L M Mulligan, D P Smith, et al.
Contributions to Nephrology|January 1, 1997
The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical managementH P Neumann, B U Bender, W Schultze-Seemann, et al.
American Journal of Human Genetics|December 1, 1994
Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinomaJ M Whaley, J Naglich, L Gelbert, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, 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.
Journal of Medical Genetics|August 3, 2001
VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortalityB U Bender, C Eng, M Olschewski, et al.
Journal of the American Society of Nephrology : JASN|May 1, 1996
Identification of 17 mutations in ten exons in the COL4A5 collagen gene, but no mutations found in four exons in COL4A6: a study of 250 patients with hematuria and suspected of having Alport syndromeN Heiskari, X Zhang, J Zhou, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumorsD J Marsh, Z Zheng, A Arnold, et al.
Oncogene|May 18, 1999
Novel mutations of the MET proto-oncogene in papillary renal carcinomasL Schmidt, K Junker, N Nakaigawa, et al.
Pageof 12