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Cancer Genetics and Cytogenetics|September 23, 2003
Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancerKouji Banno, Nobuyuki Susumu, Takeshi Hirao, et al.International Journal of Clinical Oncology|September 18, 2004
Association of HNPCC and endometrial cancersKouji Banno, Nobuyuki Susumu, Megumi Yanokura, et al.Journal of Human Genetics|October 14, 2004
Detection of allelic imbalance in the gene expression of hMSH2 or RB1 in lymphocytes from pedigrees of hereditary, nonpolyposis, colorectal cancer and retinoblastoma by an RNA difference plotYoshinori Murakami, Kana Isogai, Hiroyuki Tomita, et al.The Journal of Clinical Endocrinology and Metabolism|September 14, 2016
Age- and Gender-Specific Risk of Thyroid Cancer in Patients With Familial Adenomatous PolyposisShinya Uchino, Hideki Ishikawa, Akira Miyauchi, et al.Studies in Health Technology and Informatics|January 4, 2018
System Development Aiming Efficient Recording of Pedigree Information and Database Construction for Genetic Counseling ClinicTakuya Nagasawa, Mitsuhiro Azuma, Michihiko Aki, et al.Journal of Hepato-Biliary-Pancreatic Sciences|October 24, 2021
Clinical characteristics of pancreatic and biliary tract cancers associated with Lynch syndromeShigemasa Takamizawa, Chigusa Morizane, Noriko Tanabe, et al.Endocrine Journal|July 14, 2017
Atypical pituitary adenoma with MEN1 somatic mutation associated with abnormalities of DNA mismatch repair genes; MLH1 germline mutation and MSH6 somatic mutationShinsuke Uraki, Hiroyuki Ariyasu, Asako Doi, et al.Genes, Chromosomes & Cancer|December 4, 2002
Methylation profile of the MLH1 promoter region and their relationship to colorectal carcinogenesisYasuyuki Miyakura, Kokichi Sugano, Fumio Konishi, et al.Histopathology|November 30, 2016
Cytoplasmic MSH2 immunoreactivity in a patient with Lynch syndrome with an EPCAM-MSH2 fusionShigeki Sekine, Reiko Ogawa, Shinya Saito, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|May 16, 2003
[Basic studies on mutation analysis of K-ras codon 12 by use of three-dimensional microarray system]Masato Maekawa, Terumi Taniguchi, Chika Tatebayashi, et al.Pageof 12