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Journal Article
Gut, ISSN 0017-5749, 05/2010, Volume 59, Issue 5, pp. 666 - 689
Journal Article
Journal Article
Endoscopy, ISSN 0013-726X, 03/2008, Volume 27, Issue 2, pp. 159 - 163
Abstract BACKGROUND AND STUDY AIMS: In an ongoing screening study of 68 306 patients for early detection of colorectal cancer, those with a positive Hemoccult... 
Original Article | COLONOSCOPY | SURGERY | RECTOSIGMOIDOSCOPY | GASTROENTEROLOGY AND HEPATOLOGY | FECAL OCCULT BLOOD | COLORECTAL-CANCER | Rectal Neoplasms - diagnosis | Adenoma - diagnosis | Sigmoidoscopy | Humans | Middle Aged | Sensitivity and Specificity | Barium Sulfate | Carcinoma - diagnosis | Occult Blood | Sigmoid Neoplasms - diagnosis | Enema
Journal Article
Familial Cancer, ISSN 1389-9600, 1/2018, Volume 17, Issue 1, pp. 71 - 77
Lynch syndrome is an autosomal dominant condition caused by pathogenic mutations in the DNA mismatch repair (MMR) genes. Although commonly associated with... 
Human Genetics | Biomedicine, general | Biomedicine | Chromosomal deletion | Colorectal cancer | Cancer Research | Epidemiology | Prostate cancer | Lynch syndrome | MICRODELETION | DIAGNOSIS | ONCOLOGY | GENETICS & HEREDITY | CANCER PREDISPOSITION | INTERSTITIAL DELETION | CHG ARRAYS | Neoplasms, Multiple Primary - surgery | Genetic Testing | Neoplasms, Multiple Primary - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Middle Aged | Male | Colectomy | Prostatic Neoplasms - diagnosis | Sigmoid Neoplasms - diagnosis | Intellectual Disability - genetics | Sigmoid Neoplasms - genetics | Chromosomes, Human, Pair 2 - genetics | Adenocarcinoma - diagnosis | Prostatic Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Gene Deletion | Germ-Line Mutation | Sigmoid Neoplasms - surgery | Adenocarcinoma - genetics | Adenocarcinoma - surgery | Neoplasms, Multiple Primary - diagnosis | Anopheles | Genetic disorders | Analysis | Genes | Genetic research | Single nucleotide polymorphisms | Shiites | Genetic screening | Adenocarcinoma | Chromosome 19 | Congenital defects | Intellectual disabilities | Copy number | Familial adenomatous polyposis | Anastomosis | MSH2 protein | Chromosome deletion | Single-nucleotide polymorphism | Gene deletion | DNA repair | Chromosome 2 | Literature reviews | MSH6 protein | Cyclin-dependent kinase inhibitor p21 | Clonal deletion | Mismatch repair | Mutation | Hyperpigmentation | Brachydactyly | prostate cancer | chromosomal deletion | colorectal cancer
Journal Article
Gan to kagaku ryoho. Cancer & chemotherapy, ISSN 0385-0684, 04/2019, Volume 46, Issue 4, p. 727
We report a rare case ofrectal neuroendocrine carcinoma(NEC)following sigmoidectomy of sigmoid colon cancer. NEC of the rectum is a rare disease. It has an... 
Rectal Neoplasms - diagnosis | Carcinoma, Neuroendocrine - diagnosis | Rectal Neoplasms - surgery | Humans | Neoplasm Recurrence, Local | Rectum | Aged, 80 and over | Carcinoma, Neuroendocrine - surgery | Male | Sigmoid Neoplasms - surgery | Sigmoid Neoplasms - diagnosis
Journal Article