Thibodeau SN - Search Results

1

Linkage homogeneity near the fragile X locus in normal and fragile X families.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: thibodeau sn. Genomics. 1991 Jul;10(3):576-82. doi: 10.1016/0888-7543(91)90438-k. Genomics. 1991. PMID: 1889808

2

Linkage of nonspecific X-linked mental retardation to Xq21.31.

Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN. Jedele KB, et al. Among authors: thibodeau sn. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):436-42. doi: 10.1002/ajmg.1320430166. Am J Med Genet. 1992. PMID: 1605223

3

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: thibodeau sn. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

4

Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.

Carpenter NJ, Thibodeau SN, Brown WT. Carpenter NJ, et al. Among authors: thibodeau sn. Am J Med Genet. 1991 Feb-Mar;38(2-3):349-53. doi: 10.1002/ajmg.1320380237. Am J Med Genet. 1991. PMID: 1673310

5

Genotype prediction in the fragile X syndrome.

Hirst MC, Nakahori Y, Knight SJ, Schwartz C, Thibodeau SN, Roche A, Flint TJ, Connor JM, Fryns JP, Davies KE. Hirst MC, et al. Among authors: thibodeau sn. J Med Genet. 1991 Dec;28(12):824-9. doi: 10.1136/jmg.28.12.824. J Med Genet. 1991. PMID: 1757957 Free PMC article.

6

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.

Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B, et al. Patterson MN, et al. Among authors: thibodeau sn. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

7

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.

Thibodeau SN, Dorkins HR, Faulk KR, Berry R, Smith AC, Hagerman R, King A, Davies KE. Thibodeau SN, et al. Hum Genet. 1988 Jul;79(3):219-27. doi: 10.1007/BF00366240. Hum Genet. 1988. PMID: 3402993

8

Refined gene localization for MRX7.

Tackels D, Schwartz CE, Thibodeau SN, Michels VV. Tackels D, et al. Among authors: thibodeau sn. Am J Med Genet. 1999 Jul 30;85(3):288-9. doi: 10.1002/(sici)1096-8628(19990730)85:3<288::aid-ajmg20>3.0.co;2-y. Am J Med Genet. 1999. PMID: 10398245 No abstract available.

9

Carrier identification of cystic fibrosis by recombinant DNA techniques.

Dawson DB, Cummins LA, Schaid DJ, Michels VV, Gordon H, O'Connell EJ, Thibodeau SN. Dawson DB, et al. Among authors: thibodeau sn. Mayo Clin Proc. 1989 Mar;64(3):325-34. doi: 10.1016/s0025-6196(12)65252-5. Mayo Clin Proc. 1989. PMID: 2564899 Review.

10

Evidence for a prostate cancer susceptibility locus on the X chromosome.

Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, Visakorpi T, Kallioniemi OP, Berry R, Schaid D, French A, McDonnell S, Schroeder J, Blute M, Thibodeau S, Grönberg H, Emanuelsson M, Damber JE, Bergh A, Jonsson BA, Smith J, Bailey-Wilson J, Carpten J, Stephan D, Gillanders E, Amundson I, Kainu T, Freas-Lutz D, Baffoe-Bonnie A, Van Aucken A, Sood R, Collins F, Brownstein M, Trent J. Xu J, et al. Nat Genet. 1998 Oct;20(2):175-9. doi: 10.1038/2477. Nat Genet. 1998. PMID: 9771711

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