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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.
Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.
Boyd J, Rhei E, Federici MG, Borgen PI, Watson P, Franklin B, Karr B, Lynch J, Lemon SJ, Lynch HT. Boyd J, et al. Among authors: lynch j, lynch ht. Breast Cancer Res Treat. 1999 Jan;53(1):87-91. doi: 10.1023/a:1006030116357. Breast Cancer Res Treat. 1999. PMID: 10206076
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
Mutation of an mutL homologue in a Navajo family with hereditary nonpolyposis colorectal cancer.
Lynch HT, Drouhard T, Lanspa S, Smyrk T, Lynch P, Lynch J, Vogelstein B, Nyström-Lahti M, Sistonen P, Peltomäki P, et al. Lynch HT, et al. Among authors: lynch p, lynch j. J Natl Cancer Inst. 1994 Sep 21;86(18):1417-9. doi: 10.1093/jnci/86.18.1417. J Natl Cancer Inst. 1994. PMID: 8072036 No abstract available.
Failure to diagnose hereditary colorectal cancer and its medicolegal implications: a hereditary nonpolyposis colorectal cancer case.
Lynch HT, Paulson J, Severin M, Lynch J, Lynch P. Lynch HT, et al. Among authors: lynch j, lynch p. Dis Colon Rectum. 1999 Jan;42(1):31-5. doi: 10.1007/BF02235179. Dis Colon Rectum. 1999. PMID: 10211517
An update of HNPCC (Lynch syndrome).
Lynch HT, Smyrk T, Lynch J. Lynch HT, et al. Among authors: lynch j. Cancer Genet Cytogenet. 1997 Jan;93(1):84-99. doi: 10.1016/s0165-4608(96)00290-7. Cancer Genet Cytogenet. 1997. PMID: 9062584 Review.
Genetic counseling in a Navajo hereditary nonpolyposis colorectal cancer kindred.
Lynch HT, Drouhard T, Vasen HF, Cavalieri J, Lynch J, Nord S, Smyrk T, Lanspa S, Murphy P, Whelan KL, Peters J, de la Chapelle A. Lynch HT, et al. Among authors: lynch j. Cancer. 1996 Jan 1;77(1):30-5. doi: 10.1002/(SICI)1097-0142(19960101)77:1<30::AID-CNCR7>3.0.CO;2-R. Cancer. 1996. PMID: 8630936
Hereditary cancer in adults.
Lynch HT, Fusaro RM, Lynch J. Lynch HT, et al. Among authors: lynch j. Cancer Detect Prev. 1995;19(3):219-33. Cancer Detect Prev. 1995. PMID: 7750110 Review.
Update on the differential diagnosis, surveillance and management of hereditary non-polyposis colorectal cancer.
Lynch HT, Smyrk T, Lynch J, Fitzgibbons R Jr, Lanspa S, McGinn T. Lynch HT, et al. Among authors: lynch j. Eur J Cancer. 1995 Jul-Aug;31A(7-8):1039-46. doi: 10.1016/0959-8049(95)00126-4. Eur J Cancer. 1995. PMID: 7576988 Review.
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II). Genetics, pathology, natural history, and cancer control, Part I.
Lynch HT, Lanspa S, Smyrk T, Boman B, Watson P, Lynch J. Lynch HT, et al. Among authors: lynch j. Cancer Genet Cytogenet. 1991 Jun;53(2):143-60. doi: 10.1016/0165-4608(91)90093-a. Cancer Genet Cytogenet. 1991. PMID: 1648437 Review.
It is heterogeneous and appears to be delineated into two clinical subsets, Lynch syndromes I and II. Lynch syndrome I is characterized by an autosomal dominantly inherited proclivity to early onset colonic cancer with proximal predominance and an excess of multiple …
It is heterogeneous and appears to be delineated into two clinical subsets, Lynch syndromes I and II. Lynch syndrome I is char …
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