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Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
Nolin SL, Brown WT, Glicksman A, Houck GE Jr, Gargano AD, Sullivan A, Biancalana V, Bröndum-Nielsen K, Hjalgrim H, Holinski-Feder E, Kooy F, Longshore J, Macpherson J, Mandel JL, Matthijs G, Rousseau F, Steinbach P, Väisänen ML, von Koskull H, Sherman SL. Nolin SL, et al. Among authors: houck ge jr. Am J Hum Genet. 2003 Feb;72(2):454-64. doi: 10.1086/367713. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529854 Free PMC article.
FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males.
Nolin SL, Houck GE Jr, Gargano AD, Blumstein H, Dobkin CS, Brown WT. Nolin SL, et al. Among authors: houck ge jr. Am J Hum Genet. 1999 Sep;65(3):680-8. doi: 10.1086/302543. Am J Hum Genet. 1999. PMID: 10441574 Free PMC article.
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies.
Jenkins EC, Wen GY, Kim KS, Zhong N, Sapienza VJ, Hong H, Chen J, Li SY, Houck GE Jr, Ding X, Nolin SL, Dobkin CS, Brown WT. Jenkins EC, et al. Among authors: houck ge jr. Am J Med Genet. 1999 Apr 2;83(4):342-6. doi: 10.1002/(sici)1096-8628(19990402)83:4<342::aid-ajmg24>3.0.co;2-h. Am J Med Genet. 1999. PMID: 10208177
Familial transmission of the FMR1 CGG repeat.
Nolin SL, Lewis FA 3rd, Ye LL, Houck GE Jr, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Brown WT. Nolin SL, et al. Among authors: houck ge jr. Am J Hum Genet. 1996 Dec;59(6):1252-61. Am J Hum Genet. 1996. PMID: 8940270 Free PMC article.
Reverse mutations in the fragile X syndrome.
Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC. Brown WT, et al. Among authors: houck ge jr. Am J Med Genet. 1996 Aug 9;64(2):287-92. doi: 10.1002/(SICI)1096-8628(19960809)64:2<287::AID-AJMG11>3.0.CO;2-B. Am J Med Genet. 1996. PMID: 8844067
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselors.
Berliner JL, Shapiro FN, Nolin SL, Houck GE Jr, Ding XH, Dobkin C, Brooks SS, Brown WT. Berliner JL, et al. Among authors: houck ge jr. J Genet Couns. 1994 Sep;3(3):233-44. doi: 10.1007/BF01412229. J Genet Couns. 1994. PMID: 24234009
Mosaicism in fragile X affected males.
Nolin SL, Glicksman A, Houck GE Jr, Brown WT, Dobkin CS. Nolin SL, et al. Among authors: houck ge jr. Am J Med Genet. 1994 Jul 15;51(4):509-12. doi: 10.1002/ajmg.1320510444. Am J Med Genet. 1994. PMID: 7943031
Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 gene.
Jenkins EC, Morys I, Henderson J, Genovese M, Carter M, Li SY, Houck GE Jr, Ding X, Stark-Houck SL, Dobkin CS, et al. Jenkins EC, et al. Among authors: houck ge jr. Am J Med Genet. 1994 Jul 15;51(4):436-42. doi: 10.1002/ajmg.1320510426. Am J Med Genet. 1994. PMID: 7943013
Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
Zhong N, Liu X, Gou S, Houck GE Jr, Li S, Dobkin C, Brown WT. Zhong N, et al. Among authors: houck ge jr. Am J Med Genet. 1994 Jul 15;51(4):417-22. doi: 10.1002/ajmg.1320510423. Am J Med Genet. 1994. PMID: 7943010
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.
Brown WT, Houck GE Jr, Jeziorowska A, Levinson FN, Ding X, Dobkin C, Zhong N, Henderson J, Brooks SS, Jenkins EC. Brown WT, et al. Among authors: houck ge jr. JAMA. 1993 Oct 6;270(13):1569-75. JAMA. 1993. PMID: 8371467
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