Lindor NM - Search Results

1

Cancer Risks for PMS2-Associated Lynch Syndrome.

Ten Broeke SW, van der Klift HM, Tops CMJ, Aretz S, Bernstein I, Buchanan DD, de la Chapelle A, Capella G, Clendenning M, Engel C, Gallinger S, Gomez Garcia E, Figueiredo JC, Haile R, Hampel HL, Hopper JL, Hoogerbrugge N, von Knebel Doeberitz M, Le Marchand L, Letteboer TGW, Jenkins MA, Lindblom A, Lindor NM, Mensenkamp AR, Møller P, Newcomb PA, van Os TAM, Pearlman R, Pineda M, Rahner N, Redeker EJW, Olderode-Berends MJW, Rosty C, Schackert HK, Scott R, Senter L, Spruijt L, Steinke-Lange V, Suerink M, Thibodeau S, Vos YJ, Wagner A, Winship I, Hes FJ, Vasen HFA, Wijnen JT, Nielsen M, Win AK. Ten Broeke SW, et al. Among authors: lindor nm. J Clin Oncol. 2018 Oct 10;36(29):2961-2968. doi: 10.1200/JCO.2018.78.4777. Epub 2018 Aug 30. J Clin Oncol. 2018. PMID: 30161022 Free PMC article.

2

A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.

Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. Lindor NM, et al. Mayo Clin Proc. 1992 Aug;67(8):791-9. doi: 10.1016/s0025-6196(12)60805-2. Mayo Clin Proc. 1992. PMID: 1434919 Review.

3

Mutations in the RET protooncogene in sporadic pheochromocytomas.

Lindor NM, Honchel R, Khosla S, Thibodeau SN. Lindor NM, et al. J Clin Endocrinol Metab. 1995 Feb;80(2):627-9. doi: 10.1210/jcem.80.2.7852530. J Clin Endocrinol Metab. 1995. PMID: 7852530

4

Eight novel polymorphisms in the dystrophin gene of African-Americans: the rate of polymorphism is high.

Lindor NM, Sommer SS, Sobell J, Heston L, Thibodeau SN. Lindor NM, et al. Hum Mutat. 1993;2(6):485-8. doi: 10.1002/humu.1380020610. Hum Mutat. 1993. PMID: 7906594 No abstract available.

5

Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenics.

Lindor NM, Sobell JL, Heston LL, Thibodeau SN, Sommer SS. Lindor NM, et al. Am J Med Genet. 1994 Mar 15;54(1):1-4. doi: 10.1002/ajmg.1320540102. Am J Med Genet. 1994. PMID: 7909988

6

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.

Ledger GA, Khosla S, Lindor NM, Thibodeau SN, Gharib H. Ledger GA, et al. Among authors: lindor nm. Ann Intern Med. 1995 Jan 15;122(2):118-24. doi: 10.7326/0003-4819-122-2-199501150-00008. Ann Intern Med. 1995. PMID: 7992986 Review.

7

Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16.

Lindor NM, Jalal SM, Thibodeau SN, Bonde D, Sauser KL, Karnes PS. Lindor NM, et al. Clin Genet. 1993 Oct;44(4):185-9. doi: 10.1111/j.1399-0004.1993.tb03876.x. Clin Genet. 1993. PMID: 8261647

8

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.

Moslein G, Tester DJ, Lindor NM, Honchel R, Cunningham JM, French AJ, Halling KC, Schwab M, Goretzki P, Thibodeau SN. Moslein G, et al. Among authors: lindor nm. Hum Mol Genet. 1996 Sep;5(9):1245-52. doi: 10.1093/hmg/5.9.1245. Hum Mol Genet. 1996. PMID: 8872463

9

Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes.

Thibodeau SN, French AJ, Roche PC, Cunningham JM, Tester DJ, Lindor NM, Moslein G, Baker SM, Liskay RM, Burgart LJ, Honchel R, Halling KC. Thibodeau SN, et al. Among authors: lindor nm. Cancer Res. 1996 Nov 1;56(21):4836-40. Cancer Res. 1996. PMID: 8895729

10

Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance.

Heshmati HM, Gharib H, Khosla S, Abu-Lebdeh HS, Lindor NM, Thibodeau SN. Heshmati HM, et al. Among authors: lindor nm. Mayo Clin Proc. 1997 May;72(5):430-6. doi: 10.4065/72.5.430. Mayo Clin Proc. 1997. PMID: 9146685

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