Pages that link to "Q54622109"
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The following pages link to Hereditary gastrointestinal polyposis and nonpolyposis syndromes. (Q54622109):
Displaying 50 items.
- Family history of colorectal cancer in Iran (Q24813130) (← links)
- Clinical Genetic Testing in Gastroenterology (Q26749157) (← links)
- Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer (Q28145150) (← links)
- Use of NSAIDs for the Chemoprevention of Colorectal Cancer (Q28165741) (← links)
- In utero and neonatal sensitivity of ApcMin/+ mice to radiation-induced intestinal neoplasia (Q28591155) (← links)
- NF-kappaB in cancer: from innocent bystander to major culprit (Q29614603) (← links)
- Genes driving the colonoscope. (Q30470281) (← links)
- Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation (Q33566604) (← links)
- Soft tissue sarcoma of the extremities. A multimodality diagnostic and therapeutic approach (Q33585746) (← links)
- Gastrointestinal polyposis syndromes (Q33599177) (← links)
- Colorectal cancer: from prevention to personalized medicine. (Q33735234) (← links)
- Recognition and management of childhood cancer syndromes: a systems approach (Q33772586) (← links)
- Calcium and vitamin D. Their potential roles in colon and breast cancer prevention (Q33834317) (← links)
- Nuchal fibroma should be recognized as a new extracolonic manifestation of Gardner-variant familial adenomatous polyposis (Q33930547) (← links)
- Diagnostic yield of repeat capsule endoscopy and the effect on subsequent patient management (Q34053325) (← links)
- Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated? (Q34083348) (← links)
- A molecular rationale for the how, when and why of colorectal cancer screening (Q34206169) (← links)
- Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes (Q34283507) (← links)
- Cancer genetics in oncology practice (Q34346199) (← links)
- Cancer chemoprevention by dietary constituents: a tale of failure and promise (Q34571992) (← links)
- Screening for colon cancer and evaluation of chemoprevention with coxibs (Q34626113) (← links)
- Familial Adenomatous Polyposis—Rendering a Diagnosis Based on Recognition of an Unusual Primary Thyroid Neoplasm (Q34665064) (← links)
- Preventive gastrectomy in patients with gastric cancer risk due to genetic alterations of the E-cadherin gene defect (Q35104976) (← links)
- Gastrointestinal Inherited Polyposis Syndromes (Q35105998) (← links)
- Skin signs of gastrointestinal disease (Q35133457) (← links)
- Diagnostic values of dual focus narrow band imaging and probe-based confocal laser endomicroscopy in FAP-related duodenal adenoma (Q35830202) (← links)
- Harnessing the potential of cancer genetics in healthcare (Q35909599) (← links)
- The hamartomatous polyposis syndromes: a clinical and molecular review (Q36018533) (← links)
- The TNF family member APRIL promotes colorectal tumorigenesis (Q36311159) (← links)
- Colon cancer: polyps, prevention, and politics (Q36372079) (← links)
- Laser photoablation of ileal reservoir adenomas (Q36830986) (← links)
- Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome (Q37324996) (← links)
- Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. (Q37351692) (← links)
- Familial Adenomatous Polyposis in Children and Adolescents (Q37784375) (← links)
- Malignant tumors associated with juvenile polyposis syndrome in Japan (Q38760494) (← links)
- Colorectal cancer: Future population screening for early colorectal cancer (Q40423899) (← links)
- Molecular foundations of cancer: New targets for intervention (Q40429882) (← links)
- Progress against cancer (Q40434039) (← links)
- Genetics of follicular thyroid cancer. (Q40975265) (← links)
- Colorectal cancer: etiologic and clinical aspects (Q41145165) (← links)
- Monoallelic mutation analysis (MAMA) for identifying germline mutations (Q41306100) (← links)
- Mismatch Repair Deficiency in Phenotypically Normal Human Cells (Q41347026) (← links)
- Inheritance and susceptibility to tumours of the large bowel: a new classification of colorectal malignancies. (Q41352120) (← links)
- Risk factors for the development of colorectal carcinoma and their modification (Q41563167) (← links)
- Mutated K-ras(Asp12) promotes tumourigenesis in Apc(Min) mice more in the large than the small intestines, with synergistic effects between K-ras and Wnt pathways. (Q43274553) (← links)
- Effect of a propolis extract and caffeic acid phenethyl ester on formation of aberrant crypt foci and tumors in the rat colon. (Q44258678) (← links)
- Synchronous primary carcinomas of the ampulla of Vater and ascending colon in a patient with multiple flat adenomas (Q44723270) (← links)
- Value of the congenital hypertrophy of the retinal pigment epithelium in the diagnosis of familial adenomatous polyposis (Q45004840) (← links)
- Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer families (Q46764474) (← links)
- Colorectal cancer screening and familial risk: a survey of internal medicine residents' knowledge and practice patterns (Q47815598) (← links)