214 related articles for article (PubMed ID: 16337617)
21. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL
Hum Mol Genet; 1996 Mar; 5(3):319-30. PubMed ID: 8852655
[TBL] [Abstract][Full Text] [Related]
22. The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency.
Voorhuis M; Onland-Moret NC; Janse F; Ploos van Amstel HK; Goverde AJ; Lambalk CB; Laven JS; van der Schouw YT; Broekmans FJ; Fauser BC;
Hum Reprod; 2014 Jul; 29(7):1585-93. PubMed ID: 24812319
[TBL] [Abstract][Full Text] [Related]
23. Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.
Tejada MI; García-Alegría E; Bilbao A; Martínez-Bouzas C; Beristain E; Poch M; Ramos-Arroyo MA; López B; Fernandez Carvajal I; Ribate MP; Ramos F
Menopause; 2008; 15(5):945-9. PubMed ID: 18427356
[TBL] [Abstract][Full Text] [Related]
24. Analysis of CGG variation through 642 meioses in Fragile X families.
Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.
Yrigollen CM; Durbin-Johnson B; Gane L; Nelson DL; Hagerman R; Hagerman PJ; Tassone F
Genet Med; 2012 Aug; 14(8):729-36. PubMed ID: 22498846
[TBL] [Abstract][Full Text] [Related]
28. Transmission of the FRAXA haplotype from three nonpenetrant brothers to their affected grandsons: an update with AGG interspersion analysis.
Mogk RL; Carson NL; Chudley AE; Dawson AJ
Am J Med Genet; 1998 Jan; 75(1):28-34. PubMed ID: 9450853
[TBL] [Abstract][Full Text] [Related]
29. Does the presence of AGG interruptions within the CGG repeat tract have a protective effect on the fertility phenotype of female FMR1 premutation carriers?
Friedman-Gohas M; Kirshenbaum M; Michaeli A; Domniz N; Elizur S; Raanani H; Orvieto R; Cohen Y
J Assist Reprod Genet; 2020 Apr; 37(4):849-854. PubMed ID: 32096109
[TBL] [Abstract][Full Text] [Related]
30. Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother-newborn pairs from the general population.
Lévesque S; Dombrowski C; Morel ML; Rehel R; Côté JS; Bussières J; Morgan K; Rousseau F
Clin Genet; 2009 Dec; 76(6):511-23. PubMed ID: 19863547
[TBL] [Abstract][Full Text] [Related]
31. Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.
Nolin SL; Sah S; Glicksman A; Sherman SL; Allen E; Berry-Kravis E; Tassone F; Yrigollen C; Cronister A; Jodah M; Ersalesi N; Dobkin C; Brown WT; Shroff R; Latham GJ; Hadd AG
Am J Med Genet A; 2013 Apr; 161A(4):771-8. PubMed ID: 23444167
[TBL] [Abstract][Full Text] [Related]
32. Screen for expanded FMR1 alleles in patients with essential tremor.
Garcia Arocena D; Louis ED; Tassone F; Gilliam TC; Ottman R; Jacquemont S; Hagerman PJ
Mov Disord; 2004 Aug; 19(8):930-3. PubMed ID: 15300658
[TBL] [Abstract][Full Text] [Related]
33. Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study.
Rohr J; Allen EG; Charen K; Giles J; He W; Dominguez C; Sherman SL
Hum Reprod; 2008 May; 23(5):1220-5. PubMed ID: 18310677
[TBL] [Abstract][Full Text] [Related]
34. Evaluating the clinical utility of a long-read sequencing-based approach in genetic testing of fragile-X syndrome.
Hou F; Mao A; Shan S; Li Y; Meng W; Zhan J; Nie W; Jin H
Clin Chim Acta; 2023 Nov; 551():117614. PubMed ID: 38375623
[TBL] [Abstract][Full Text] [Related]
35. Correlation of triple repeats on the FMR1 (fragile X) gene to ovarian reserve: a new infertility test?
Gleicher N; Weghofer A; Oktay K; Barad DH
Acta Obstet Gynecol Scand; 2009; 88(9):1024-30. PubMed ID: 19642041
[TBL] [Abstract][Full Text] [Related]
36. Single nucleotide polymorphism and FMR1 CGG repeat instability in two Basque valleys.
Barasoain M; Barrenetxea G; Ortiz-Lastra E; González J; Huerta I; Télez M; Ramírez JM; Domínguez A; Gurtubay P; Criado B; Arrieta I
Ann Hum Genet; 2012 Mar; 76(2):110-20. PubMed ID: 22211843
[TBL] [Abstract][Full Text] [Related]
37. A new insight into fragile X syndrome among Basque population.
Peñagarikano O; Gil A; Télez M; Ortega B; Flores P; Veiga I; Peixoto A; Criado B; Arrieta I
Am J Med Genet A; 2004 Jul; 128A(3):250-5. PubMed ID: 15216545
[TBL] [Abstract][Full Text] [Related]
38. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.
Loesch DZ; Bui QM; Huggins RM; Mitchell RJ; Hagerman RJ; Tassone F
J Med Genet; 2007 Mar; 44(3):200-4. PubMed ID: 16905681
[TBL] [Abstract][Full Text] [Related]
39. Rearrangements in the flanking sequences of the triplet repeat of the FMR1 gene give clues to the mechanisms involved in repeat instability in fragile X.
Mononen T; von Koskull H; Airaksinen RL; Juvonen V
DNA Repair (Amst); 2008 May; 7(5):684-5. PubMed ID: 18337192
[No Abstract] [Full Text] [Related]
40. Screening for fragile X syndrome among Brazilian mentally retarded male patients using PCR from buccal cell DNA.
Christofolini DM; Lipay MV; Ramos MA; Brunoni D; Melaragno MI
Genet Mol Res; 2006 Jul; 5(3):448-53. PubMed ID: 17117359
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
