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Specific genetic change in tumors associated with von Hippel-Lindau disease.
Tory K, Brauch H, Linehan M, Barba D, Oldfield E, Filling-Katz M, Seizinger B, Nakamura Y, White R, Marshall FF, et al. Tory K, et al. Among authors: brauch h. J Natl Cancer Inst. 1989 Jul 19;81(14):1097-101. doi: 10.1093/jnci/81.14.1097. J Natl Cancer Inst. 1989. PMID: 2738940
[Molecular diagnosis of the Hippel-Lindau syndrome].
Neumann HP, Brauch H. Neumann HP, et al. Among authors: brauch h. Dtsch Med Wochenschr. 1995 Oct 13;120(41):1416. Dtsch Med Wochenschr. 1995. PMID: 7555669 German. No abstract available.
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.
Decker HJ, Neuhaus C, Jauch A, Speicher M, Ried T, Bujard M, Brauch H, Störkel S, Stöckle M, Seliger B, Huber C. Decker HJ, et al. Among authors: brauch h. Hum Genet. 1996 Jun;97(6):770-6. doi: 10.1007/BF02346188. Hum Genet. 1996. PMID: 8641695
331 results