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American Journal of Respiratory and Critical Care Medicine|February 27, 2007
Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndromeJorge R Toro, Stephen E Pautler, Laveta Stewart, et al.
American Journal of Human Genetics|April 27, 2005
Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndromeLaura S Schmidt, Michael L Nickerson, Michelle B Warren, et al.
American Journal of Human Genetics|May 29, 2003
Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North AmericaJorge R Toro, Michael L Nickerson, Ming-Hui Wei, et al.
Nature Communications|June 20, 2020
The genomic and epigenomic evolutionary history of papillary renal cell carcinomasBin Zhu, Maria Luana Poeta, Manuela Costantini, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 5, 2008
Improved identification of von Hippel-Lindau gene alterations in clear cell renal tumorsMichael L Nickerson, Erich Jaeger, Yangu Shi, et al.
Journal of the American Academy of Dermatology|July 21, 2010
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009Vinzenz Oji, Gianluca Tadini, Masashi Akiyama, et al.
Human Molecular Genetics|November 25, 2011
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinomaSummer S Han, Meredith Yeager, Lee E Moore, et al.
Human Molecular Genetics|October 20, 2011
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23Xifeng Wu, Ghislaine Scelo, Mark P Purdue, et al.
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