Thibodeau SN - Search Results

1

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.

Win AK, Dowty JG, Antill YC, English DR, Baron JA, Young JP, Giles GG, Southey MC, Winship I, Lipton L, Parry S, Thibodeau SN, Haile RW, Gallinger S, Le Marchand L, Lindor NM, Newcomb PA, Hopper JL, Jenkins MA. Win AK, et al. Among authors: thibodeau sn. Obstet Gynecol. 2011 Apr;117(4):899-905. doi: 10.1097/AOG.0b013e3182110ea3. Obstet Gynecol. 2011. PMID: 21422863 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. Among authors: thibodeau sn. 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. Among authors: thibodeau sn. 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. Among authors: thibodeau sn. 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. Among authors: thibodeau sn. 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: thibodeau sn. 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. Among authors: thibodeau sn. Clin Genet. 1993 Oct;44(4):185-9. doi: 10.1111/j.1399-0004.1993.tb03876.x. Clin Genet. 1993. PMID: 8261647

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. Among authors: thibodeau sn. 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. Among authors: thibodeau sn. 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: thibodeau sn. Hum Mol Genet. 1996 Sep;5(9):1245-52. doi: 10.1093/hmg/5.9.1245. Hum Mol Genet. 1996. PMID: 8872463

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

536 results

Search Page

Filters