Showing results (61-70 of 76) with videos related to
Sort By:
Pageof 8
Radiology|March 1, 1990
von Hippel-Lindau disease: radiologic screening for visceral manifestationsP L Choyke, M R Filling-Katz, T H Shawker, et al.Cancer Research|May 15, 1992
p53 mutations are associated with 17p allelic loss in grade II and grade III astrocytomaA von Deimling, R H Eibl, H Ohgaki, et al.Annals of Internal Medicine|January 15, 1993
Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinomaF P Li, H J Decker, B Zbar, et al.Nature|March 17, 1988
Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinomaB R Seizinger, G A Rouleau, L J Ozelius, et al.American Journal of Human Genetics|June 1, 1994
Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomasR H Lekanne Deprez, A B Bianchi, N A Groen, et al.Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.Journal of Neuropathology and Experimental Neurology|January 1, 1993
Comparative study of p53 gene and protein alterations in human astrocytic tumorsD N Louis, A von Deimling, R Y Chung, et al.Nature|September 17, 1987
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22G A Rouleau, W Wertelecki, J L Haines, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.Pageof 8