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Toward a consensus in molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome).
Lynch HT, Lynch JF, Lynch PM. Lynch HT, et al. Among authors: lynch jf, lynch pm. J Natl Cancer Inst. 2007 Feb 21;99(4):261-3. doi: 10.1093/jnci/djk077. J Natl Cancer Inst. 2007. PMID: 17312298 No abstract available.
Upper gastrointestinal manifestations in families with hereditary flat adenoma syndrome.
Lynch HT, Smyrk TC, Lanspa SJ, Jenkins JX, Lynch PM, Cavalieri J, Lynch JF. Lynch HT, et al. Among authors: lynch pm, lynch jf. Cancer. 1993 May 1;71(9):2709-14. doi: 10.1002/1097-0142(19930501)71:9<2709::aid-cncr2820710904>3.0.co;2-t. Cancer. 1993. PMID: 8385563
The polyps occur at a later age (median, 55 years) compared with age at onset of polyps in patients with familial adenomatous polyposis (FAP) and patients with the Lynch syndromes. ...
The polyps occur at a later age (median, 55 years) compared with age at onset of polyps in patients with familial adenomatous polyposis (FAP …
Cyclin D1 polymorphism and increased risk of colorectal cancer at young age.
Kong S, Wei Q, Amos CI, Lynch PM, Levin B, Zong J, Frazier ML. Kong S, et al. Among authors: lynch pm. J Natl Cancer Inst. 2001 Jul 18;93(14):1106-8. doi: 10.1093/jnci/93.14.1106. J Natl Cancer Inst. 2001. PMID: 11459873 No abstract available.
Effects of cyclin D1 polymorphism on age of onset of hereditary nonpolyposis colorectal cancer.
Kong S, Amos CI, Luthra R, Lynch PM, Levin B, Frazier ML. Kong S, et al. Among authors: lynch pm. Cancer Res. 2000 Jan 15;60(2):249-52. Cancer Res. 2000. PMID: 10667569
Clinical challenges in management of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.
Lynch PM. Lynch PM. Cancer. 1999 Dec 1;86(11 Suppl):2533-9. doi: 10.1002/(sici)1097-0142(19991201)86:11+<2533::aid-cncr10>3.0.co;2-3. Cancer. 1999. PMID: 10630179 Review. No abstract available.
Hereditary nonpolyposis colorectal cancer--Lynch syndromes I and II.
Lynch HT, Lanspa SJ, Boman BM, Smyrk T, Watson P, Lynch JF, Lynch PM, Cristofaro G, Bufo P, Tauro AV, et al. Lynch HT, et al. Among authors: lynch jf, lynch pm. Gastroenterol Clin North Am. 1988 Dec;17(4):679-712. Gastroenterol Clin North Am. 1988. PMID: 3068137 Review.
HNPCC is subdivided into Lynch syndrome I, which is restricted to site-specific colon cancer susceptibility, and Lynch syndrome II, which shows all of the features of Lynch syndrome I, but in addition, patients are at inordinately increased risk for carcinoma …
HNPCC is subdivided into Lynch syndrome I, which is restricted to site-specific colon cancer susceptibility, and Lynch syndrom …
Adenocarcinoma of the small bowel in lynch syndrome II.
Lynch HT, Smyrk TC, Lynch PM, Lanspa SJ, Boman BM, Ens J, Lynch JF, Strayhorn P, Carmody T, Cristofaro G. Lynch HT, et al. Among authors: lynch pm, lynch jf. Cancer. 1989 Nov 15;64(10):2178-83. doi: 10.1002/1097-0142(19891115)64:10<2178::aid-cncr2820641033>3.0.co;2-0. Cancer. 1989. PMID: 2804907
We report adenocarcinoma of the small bowel in nine patients from eight Lynch syndrome II extended pedigrees. Each affected patient was in the direct genetic lineage or manifested multiple primary cancers (stomach, colon, endometrium, and ovary) consonant with the tumor sp …
We report adenocarcinoma of the small bowel in nine patients from eight Lynch syndrome II extended pedigrees. Each affected patient w …
A follow-up study of colonic epithelial proliferation as a biomarker ina Native-American family with hereditary nonpolyposis colon cancer.
Lynch PM, Wargovich MJ, Lynch HT, Palmer C, Lanspa S, Drouhard T, Lynch J. Lynch PM, et al. Among authors: lynch ht, lynch j. J Natl Cancer Inst. 1991 Jul 3;83(13):951-4. doi: 10.1093/jnci/83.13.951. J Natl Cancer Inst. 1991. PMID: 2067038
Phenotypic variation in colorectal adenoma/cancer expression in two families. Hereditary flat adenoma syndrome.
Lynch HT, Smyrk TC, Lanspa SJ, Lynch PM, Watson P, Strayhorn PC, Bronson EK, Lynch JF, Priluck IA, Appelman HD. Lynch HT, et al. Among authors: lynch pm, lynch jf. Cancer. 1990 Sep 1;66(5):909-15. doi: 10.1002/1097-0142(19900901)66:5<909::aid-cncr2820660516>3.0.co;2-h. Cancer. 1990. PMID: 2386918
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
Sunga AY, Ricker C, Espenschied CR, Castillo D, Melas M, Herzog J, Bannon S, Cruz-Correa M, Lynch P, Solomon I, Gruber SB, Weitzel JN. Sunga AY, et al. Among authors: lynch p. Cancer Genet. 2017 Apr;212-213:1-7. doi: 10.1016/j.cancergen.2017.01.003. Epub 2017 Feb 9. Cancer Genet. 2017. PMID: 28449805
Lynch syndrome (LS), the most common hereditary colorectal cancer syndrome, is caused by mismatch repair (MMR) gene mutations. ...
Lynch syndrome (LS), the most common hereditary colorectal cancer syndrome, is caused by mismatch repair (MMR) gene mutations. ...
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