161 related articles for article (PubMed ID: 12116303)
1. Pilot study for the neonatal screening of fragile X syndrome.
Rifé M; Mallolas J; Badenas C; Tazón B; Miguélez MR; Pàmpols T; Sànchez A; Milà M
Prenat Diagn; 2002 Jun; 22(6):459-62. PubMed ID: 12116303
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Detection of FMR-1 gene expression by RT-PCR].
Zheng L; Fan Y; Huang T; Zhu N; Shen Y; Wu G
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564
[TBL] [Abstract][Full Text] [Related]
4. [New methods for the diagnosis of fragile X syndrome: a study of the FMRP in blood and hair].
Ramos-Fuentes FJ
Rev Neurol; 2001 Oct; 33 Suppl 1():S9-S13. PubMed ID: 12447812
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular diagnosis and genetic counseling for fragile X mental retardation.
Pandey UB; Phadke SR; Mittal B
Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237
[TBL] [Abstract][Full Text] [Related]
7. Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothers.
Mueller OT; Hartsfield JK; Amar MJ; Gallardo LA; Kousseff BG
Am J Med Genet; 1995 Aug; 60(4):302-6. PubMed ID: 7485265
[TBL] [Abstract][Full Text] [Related]
8. Timing of the absence of FMR1 expression in full mutation chorionic villi.
Willemsen R; Bontekoe CJ; Severijnen LA; Oostra BA
Hum Genet; 2002 Jun; 110(6):601-5. PubMed ID: 12107447
[TBL] [Abstract][Full Text] [Related]
9. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.
Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I
Prenat Diagn; 1999 Dec; 19(13):1223-30. PubMed ID: 10660959
[TBL] [Abstract][Full Text] [Related]
10. Rare variants in the promoter of the fragile X syndrome gene (FMR1).
Milà M; Castellví-Bel S; Sánchez A; Barceló A; Badenas C; Mallolas J; Estivill X
Mol Cell Probes; 2000 Apr; 14(2):115-9. PubMed ID: 10799273
[TBL] [Abstract][Full Text] [Related]
11. [Molecular biologic screening test (PCR) for fragile X syndrome].
Kovács E; Morava E; Nádasi E; Czakó M; Melegh B; Kosztolányi G
Orv Hetil; 1998 Dec; 139(52):3121-3. PubMed ID: 9914733
[TBL] [Abstract][Full Text] [Related]
12. Molecular diagnosis of Fragile X syndrome.
Sofocleous C; Kolialexi A; Mavrou A
Expert Rev Mol Diagn; 2009 Jan; 9(1):23-30. PubMed ID: 19099346
[TBL] [Abstract][Full Text] [Related]
13. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
Mandel JL; Biancalana V
Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of expression of FMR-1 gene in male patients with fragile X syndrome using RT-PCR].
Zhu W; Li M; Zhao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Feb; 15(1):17-9. PubMed ID: 9456366
[TBL] [Abstract][Full Text] [Related]
15. Fragile X syndrome without CCG amplification has an FMR1 deletion.
Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
[TBL] [Abstract][Full Text] [Related]
16. Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.
Charalsawadi C; Sripo T; Limprasert P
J Med Assoc Thai; 2005 Aug; 88(8):1057-61. PubMed ID: 16404832
[TBL] [Abstract][Full Text] [Related]
17. The emerging fragile X premutation phenotype: evidence from the domain of social cognition.
Cornish K; Kogan C; Turk J; Manly T; James N; Mills A; Dalton A
Brain Cogn; 2005 Feb; 57(1):53-60. PubMed ID: 15629215
[TBL] [Abstract][Full Text] [Related]
18. Fragile X syndrome a case report of a family.
Chatterjee C; Guha D; Das S; Singh SK; Dasgupta U; Saha S; Bannerjee D
Indian J Pathol Microbiol; 2001 Oct; 44(4):499-502. PubMed ID: 12035381
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Plastic microchip electrophoresis for genetic screening: the analysis of polymerase chain reactions products of fragile X (CGG)n alleles.
Sung WC; Lee GB; Tzeng CC; Chen SH
Electrophoresis; 2001 Apr; 22(6):1188-93. PubMed ID: 11358146
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
