G. Glenn

发表

Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer

W. Linehan, M. Wei, B. Zbar, 2006, Journal of Medical Genetics.

Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer

P. Choyke, W. Linehan, M. Wei, 2005, Journal of Medical Genetics.

Net Exchange of CO2 in a Mid-Latitude Forest

D. Paslier, S. Wofsy, P. Bakwin, 1993, Science.

Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau disease.

S. Libutti, P. Choyke, W. Linehan, 2000, Surgery.

Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization.

L. Liotta, R. Klausner, W. Linehan, 1999, Cancer research.

Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3.

P. Choyke, M. Walther, H. Brauch, 1990, Genomics.

Imaging features of hereditary papillary renal cancers.

P. Choyke, W. Linehan, I. Lubensky, 1997, Journal of computer assisted tomography.

Familial renal oncocytoma: clinicopathological study of 5 families.

P. Choyke, W. Linehan, I. Lubensky, 1998, The Journal of urology.

Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene.

P. Choyke, W. Linehan, L. Schmidt, 1998, Cancer research.

Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer.

W. Linehan, M. Tucker, M. Merino, 2008, Archives of dermatology.