These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations. Eichler EE; Nelson DL Am J Med Genet; 1996 Jul; 64(1):220-5. PubMed ID: 8826480 [TBL] [Abstract][Full Text] [Related]
4. The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. Chen LS; Tassone F; Sahota P; Hagerman PJ Hum Mol Genet; 2003 Dec; 12(23):3067-74. PubMed ID: 14519687 [TBL] [Abstract][Full Text] [Related]
5. Facile FMR1 mRNA structure regulation by interruptions in CGG repeats. Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ Nucleic Acids Res; 2005; 33(2):451-63. PubMed ID: 15659577 [TBL] [Abstract][Full Text] [Related]
6. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia. Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; Tranebjaerg L Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563 [TBL] [Abstract][Full Text] [Related]
7. FMR1 premutation allele (CGG)81 is stable in mice. Bontekoe CJ; de Graaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA Eur J Hum Genet; 1997; 5(5):293-8. PubMed ID: 9412786 [TBL] [Abstract][Full Text] [Related]
8. The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells. de Graaff E; de Vries BB; Willemsen R; van Hemel JO; Mohkamsing S; Oostra BA; van den Ouweland AM Am J Med Genet; 1996 Aug; 64(2):302-8. PubMed ID: 8844070 [TBL] [Abstract][Full Text] [Related]
9. Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element. Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ Hum Mol Genet; 2004 Mar; 13(5):543-9. PubMed ID: 14722156 [TBL] [Abstract][Full Text] [Related]
10. Conservation of CGG region in FMR1 gene in mammals. Deelen W; Bakker C; Halley DJ; Oostra BA Am J Med Genet; 1994 Jul; 51(4):513-6. PubMed ID: 7943032 [TBL] [Abstract][Full Text] [Related]
11. Fragile X founder effects and new mutations in Finland. Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481 [TBL] [Abstract][Full Text] [Related]
12. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features. Wiegers AM; Curfs LM; Meijer H; Oostra B; Fryns JP Genet Couns; 1994; 5(4):377-80. PubMed ID: 7888141 [TBL] [Abstract][Full Text] [Related]
13. Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene. Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K Am J Med Genet; 1999 May; 84(3):229-32. PubMed ID: 10331598 [TBL] [Abstract][Full Text] [Related]
14. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population. Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; Manoli P; Holden JJ; Hettinger JA Am J Med Genet; 1999 May; 84(3):217-20. PubMed ID: 10331595 [TBL] [Abstract][Full Text] [Related]
15. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Eichler EE; Hammond HA; Macpherson JN; Ward PA; Nelson DL Hum Mol Genet; 1995 Dec; 4(12):2199-208. PubMed ID: 8634688 [TBL] [Abstract][Full Text] [Related]
16. AGG interspersion analysis of the FMR1 CGG repeats in mental retardation of unspecific cause. Poon PM; Chen QL; Zhong N; Lam ST; Lai KY; Wong CK; Pang CP Clin Biochem; 2006 Mar; 39(3):244-8. PubMed ID: 16337617 [TBL] [Abstract][Full Text] [Related]
17. A methylation PCR approach for detection of fragile X syndrome. Panagopoulos I; Lassen C; Kristoffersson U; Aman P Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261 [TBL] [Abstract][Full Text] [Related]
19. Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population. Sharma D; Gupta M; Thelma BK Genet Epidemiol; 2001 Jan; 20(1):129-144. PubMed ID: 11119302 [TBL] [Abstract][Full Text] [Related]
20. FMR1 in global populations. Kunst CB; Zerylnick C; Karickhoff L; Eichler E; Bullard J; Chalifoux M; Holden JJ; Torroni A; Nelson DL; Warren ST Am J Hum Genet; 1996 Mar; 58(3):513-22. PubMed ID: 8644711 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]