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Clinical and Laboratory Haematology|September 24, 2005
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implicationsC Wylenzek, J Trübenbach, P Gohl, et al.Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histologyV Schumacher, S Schneider, A Figge, et al.Journal of Medical Genetics|July 7, 2009
Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domainJ Chen, G Wildhardt, Z Zhong, et al.Human Mutation|October 29, 1998
Ten novel mutations found in AniridiaM T Wolf, B Lorenz, A Winterpacht, et al.British Journal of Cancer|March 6, 2015
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromesC P Kratz, L Franke, H Peters, et al.Pageof 2