Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL)-Reference-Cited by-同舟云学术

Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL)

Published:1994-10 Issue:1 Volume:77 Page:1-13
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Decker Hans-Joachim H.,Klauck Sabine M.,Lawrence Jeanne B.,McNeil John,Smith David,Gemmill Robert M.,Sandberg Avery A.,Neumann Hartmut H.P.,Simon Babette,Green Jane,Seizinger Bernd R.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference37 articles.

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3. Loss of heterozygosity on 3p in a renal cell carcinoma in von Hippel-Lindau syndrome;Decker;Cancer Genet Cytogenet,1989

4. Specific genetic change in tumors associated with von Hippel-Lindau disease;Tory;J Natl Cancer Inst,1989

5. Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma;Maher;J Med Genet,1990

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