Related Experiment Videos
Colorectal cancer and family history
1The Netherlands Foundation for the Detection of Hereditary Tumours & Department of Gastroenterology, Leiden University Medical Centre. nfdht@xs4all.nl
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A thirty-year follow-up surveillance study for neoplasia of a dutch ulcerative colitis cohort.
TheScientificWorldJournal·2014
MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology·2001
[Frequency of duodenal adenomas in patients with familial adenomatous polyposis].
Nederlands tijdschrift voor geneeskunde·2001
The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer.
Gynecologic oncology·2001
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.
Journal of medical genetics·2001
Leiomyoma of the urinary bladder.
Annales chirurgiae et gynaecologiae·2002
Lichtenstein inguinal herniorraphy under local infiltration anaesthesia as rapid outpatient procedure.
Annales chirurgiae et gynaecologiae·2002
Surgically treated adenocarcinomas of the right side of the colon during a ten year period: a retrospective study.
Annales chirurgiae et gynaecologiae·2002
Effects of glucose on collagen mRNA levels and collagen secretion in EAhy 926 endothelial cell line.
Annales chirurgiae et gynaecologiae·2002
Burst abdomen. Local synthesis of nucleic acids, glycosaminoglycans, proteins and collagen in wounds.
Annales chirurgiae et gynaecologiae·2002
Innervation of normal and hypertrophic human scars and experimental wounds in the rat.
Annales chirurgiae et gynaecologiae·2002
Novel TCOF1 Frameshift Variant and Phenotypic Heterogeneity in a Chinese Family With Treacher Collins Syndrome.
Molecular genetics & genomic medicine·2026
Estrogen insensitivity syndrome: the 'Upside Down' of ESR1 mutations.
The Journal of endocrinology·2026
[The unbearable versatility of endocrine aging].
Problemy endokrinologii·2026