Lindor NM - Search Results

1

Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.

Kastrinos F, Ojha RP, Leenen C, Alvero C, Mercado RC, Balmaña J, Valenzuela I, Balaguer F, Green R, Lindor NM, Thibodeau SN, Newcomb P, Win AK, Jenkins M, Buchanan DD, Bertario L, Sala P, Hampel H, Syngal S, Steyerberg EW; Lynch Syndrome prediction model validation study group. Kastrinos F, et al. Among authors: lindor nm. J Natl Cancer Inst. 2015 Nov 18;108(2):djv308. doi: 10.1093/jnci/djv308. Print 2016 Feb. J Natl Cancer Inst. 2015. PMID: 26582061 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

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

7

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7.

Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Olson TM, et al. Among authors: lindor nm. Hum Mol Genet. 1993 Jul;2(7):869-73. doi: 10.1093/hmg/2.7.869. Hum Mol Genet. 1993. PMID: 8364568

8

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

9

Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.

Lindor NM, Devries EM, Michels VV, Schad CR, Jalal SM, Donovan KM, Smithson WA, Kvols LK, Thibodeau SN, Dewald GW. Lindor NM, et al. Clin Genet. 1996 Mar;49(3):124-9. doi: 10.1111/j.1399-0004.1996.tb03270.x. Clin Genet. 1996. PMID: 8737976

10

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

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