35 results on '"Lynch, Henry T."'
Search Results
2. The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features
3. Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer families
4. BRCA1 and pancreatic cancer: pedigree findings and their causal relationships
5. Challenging pedigrees seen in a hereditary cancer consultation center
6. Challenging colonic polyposis pedigrees: differential diagnosis, surveillance, and management concerns
7. Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay
8. Family with acute myelocytic leukemia, breast, ovarian, and gastrointestinal cancer
9. E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinoma
10. Microsatellite Instability and Expression of MLH1 and MSH2 in Normal and Malignant Endometrial and Ovarian Epithelium in Hereditary Nonpolyposis Colorectal Cancer Family Members
11. An Update on DNA-Based BRCA1/BRCA2 Genetic Counseling in Hereditary Breast Cancer
12. Population differences in familial adenomatous polyposis may be an expression of geographic differences in APC mutation pattern
13. How early to test for a cancer-causing germline mutation
14. An update of HNPCC (Lynch syndrome)
15. Absence of germline mutations in exons 5–9 of the p53 gene in patients with Li-Fraumeni-like (SBLA) and familial adenomatous polyposis heritable cancer syndromes
16. Deletion (5q) in a desmoid tumor of a patient with Gardner's syndrome
17. Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II)
18. Hereditary malignant melanoma: A unifying etiologic hypothesis
19. Breast cancer genetics in an oncology clinic: 328 consecutive patients
20. Familial hepatocellular carcinoma in an endemic area of Thailand
21. A review of hereditary malignant melanoma including biomarkers in familial atypical multiple mole melanoma syndrome
22. α-L-fucosidase variant and lipid-associated sialic acid in hereditary ovarian cancer
23. Familial mesothelioma: Review and family study
24. Familial polyposis coli and neurofibromatosis in the same patient: A family study
25. Hereditary nonpolyposis colorectal cancer in a Navajo Indian family
26. Genetics, biomarkers, and control of breast cancer: A review
27. Hereditary ovarian cancer: Pedigree studies, part II
28. Chromosome instability and the FAMMM syndrome
29. Familial bladder cancer in an oncology clinic
30. Cancer genes, multiple primary cancer, and von Hippel-Lindau disease
31. Increased in vitro tetraploidy in dermal monolayer cultures derived from normals
32. Low serum IgA in a familial ovarian cancer aggregate
33. Genetic/epidemiological findings in a study of smoking-associated tumors
34. Breast cancer diagnosis in a putative obligate gene carrier: A family study
35. Letter to the editor: Reassignment of a cancer family syndrome gene to chromosome 18
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