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Hereditary Cancer in Clinical Practice|March 13, 2010
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patientsWaltraut Friedl, Stefan Aretz
Human Mutation|February 22, 2002
A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1Yaping Wang, Waltraut Friedl, Marlies Sengteller, et al.
European Journal of Human Genetics : EJHG|October 3, 2003
Frequency and parental origin of de novo APC mutations in familial adenomatous polyposisStefan Aretz, Siegfried Uhlhaas, Reiner Caspari, et al.
Acta Oncologica (Stockholm, Sweden)|July 27, 2007
May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?Xiaorong Liu, Xiangnian Shan, Waltraut Friedl, et al.
International Journal of Cancer|December 21, 2002
Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genesYaping Wang, Waltraut Friedl, Christof Lamberti, et al.
European Journal of Human Genetics : EJHG|May 5, 2005
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genesMaria Wehner, Elisabeth Mangold, Marlies Sengteller, et al.
Human Mutation|May 9, 2007
Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP)Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, et al.
Cancer Genetics and Cytogenetics|June 14, 2005
Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancerMing Zhu, Jintian Li, Xiaomei Zhang, et al.
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