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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 1
2003 2
2021 0
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4 results
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Page 1
Cancer risk in mismatch repair gene mutation carriers.
Watson P, Lynch HT. Watson P, et al. Fam Cancer. 2001;1(1):57-60. doi: 10.1023/a:1011590617833. Fam Cancer. 2001. PMID: 14574017 Review.
Hereditary breast-ovarian cancer at the bedside: role of the medical oncologist.
Lynch HT, Snyder CL, Lynch JF, Riley BD, Rubinstein WS. Lynch HT, et al. J Clin Oncol. 2003 Feb 15;21(4):740-53. doi: 10.1200/JCO.2003.05.096. J Clin Oncol. 2003. PMID: 12586815 Review.
Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.
Sarroca C, Peltomäki P, Alfano N, Tedesco G, Della Valle A, Dominguez A, Lynch HT. Sarroca C, et al. Cancer Genet Cytogenet. 2003 Apr 1;142(1):13-20. doi: 10.1016/s0165-4608(02)00766-5. Cancer Genet Cytogenet. 2003. PMID: 12660027
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.
Lynch HT, Brand RE, Hogg D, Deters CA, Fusaro RM, Lynch JF, Liu L, Knezetic J, Lassam NJ, Goggins M, Kern S. Lynch HT, et al. Cancer. 2002 Jan 1;94(1):84-96. doi: 10.1002/cncr.10159. Cancer. 2002. PMID: 11815963 Free article.