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Journal of Carcinogenesis|October 30, 2003
BRCA1/2 mutation screening and LOH analysis of lung adenocarcinoma tissue in a multiple-cancer patient with a strong family history of breast cancerMelanie Barbara Boettger, Consolato Sergi, Peter MeyerJournal of Pediatric Ophthalmology and Strabismus|August 13, 2004
Colobomas of the iris and choroid and high signal intensity cerebral foci on T2-weighted magnetic resonance images in Klinefelter's syndromeMelanie Barbara Boettger, Klaus Kirchhof, Consolato Sergi, et al.International Journal of Cancer|June 10, 2003
Exclusion of BRAFV599E as a melanoma susceptibility mutationPeter Meyer, Ruediger Klaes, Christina Schmitt, et al.International Journal of Cancer|April 29, 2006
ARLTS1 variants and melanoma riskBernd Frank, Peter Meyer, Melanie Barbara Boettger, et al.Melanoma Research|May 15, 2007
Molecular genetic analysis of NBS1 in German melanoma patientsPeter Meyer, Henrike Stapelmann, Bernd Frank, et al.Nature Genetics|May 29, 2002
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaRoxanne Y Walder, Daniel Landau, Peter Meyer, et al.Cancer Research|September 7, 2007
Seizure 6-like (SEZ6L) gene and risk for lung cancerIvan P Gorlov, Peter Meyer, Triantafillos Liloglou, et al.Pageof 1