125 related articles for article (PubMed ID: 9063737)
1. The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.
Murray A; Macpherson JN; Pound MC; Sharrock A; Youings SA; Dennis NR; McKechnie N; Linehan P; Morton NE; Jacobs PA
Hum Mol Genet; 1997 Feb; 6(2):173-84. PubMed ID: 9063737
[TBL] [Abstract][Full Text] [Related]
2. Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.
Murray A; Youings S; Dennis N; Latsky L; Linehan P; McKechnie N; Macpherson J; Pound M; Jacobs P
Hum Mol Genet; 1996 Jun; 5(6):727-35. PubMed ID: 8776586
[TBL] [Abstract][Full Text] [Related]
3. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males.
Barros Santos C; Gonçalves Pimentel MM
Int J Mol Med; 2003 Sep; 12(3):385-9. PubMed ID: 12883656
[TBL] [Abstract][Full Text] [Related]
4. FRAXA and FRAXE: the results of a five year survey.
Youings SA; Murray A; Dennis N; Ennis S; Lewis C; McKechnie N; Pound M; Sharrock A; Jacobs P
J Med Genet; 2000 Jun; 37(6):415-21. PubMed ID: 10851251
[TBL] [Abstract][Full Text] [Related]
5. Studies of FRAXA and FRAXE in women with premature ovarian failure.
Murray A; Webb J; Grimley S; Conway G; Jacobs P
J Med Genet; 1998 Aug; 35(8):637-40. PubMed ID: 9719368
[TBL] [Abstract][Full Text] [Related]
6. Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease.
Costa A; Gao L; Carrillo F; Cáceres-Redondo MT; Carballo M; Díaz-Martín J; Gómez-Garre P; Sobrino F; Lucas M; López-Barneo J; Mir P; Pintado E
Parkinsonism Relat Disord; 2011 May; 17(4):281-4. PubMed ID: 21257332
[TBL] [Abstract][Full Text] [Related]
7. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M
Am J Med Genet; 1999 May; 84(3):184-90. PubMed ID: 10331587
[TBL] [Abstract][Full Text] [Related]
8. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
Brown TC; Tarleton JC; Go RC; Longshore JW; Descartes M
Am J Med Genet; 1997 Dec; 73(4):447-55. PubMed ID: 9415473
[TBL] [Abstract][Full Text] [Related]
9. A survey of FRAXE allele sizes in three populations.
Zhong N; Ju W; Curley D; Wang D; Pietrofesa J; Wu G; Shen Y; Pang C; Poon P; Liu X; Gou S; Kajanoja E; Ryynänen M; Dobkin C; Brown WT
Am J Med Genet; 1996 Aug; 64(2):415-9. PubMed ID: 8844095
[TBL] [Abstract][Full Text] [Related]
10. FRAXE intermediate alleles are associated with Parkinson's disease.
Annesi G; Nicoletti G; Tarantino P; Cutuli N; Annesi F; Marco EV; Zappia M; Morgante L; Arabia G; Pugliese P; Condino F; Carrideo S; Civitelli D; Caracciolo M; Romeo N; Spadafora P; Candiano IC; Quattrone A
Neurosci Lett; 2004 Sep; 368(1):21-4. PubMed ID: 15342126
[TBL] [Abstract][Full Text] [Related]
11. Stability and haplotype analysis of the FRAXE region.
Murray A; Ennis S; Youings SA; Sharrock AJ; Lewis C; Pound MC; Macpherson JN; Dennis NR; Morton NE; Jacobs PA
Eur J Hum Genet; 2000 Aug; 8(8):583-9. PubMed ID: 10951520
[TBL] [Abstract][Full Text] [Related]
12. DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome.
Chan SY; Wong V
Clin Genet; 1998 Mar; 53(3):179-83. PubMed ID: 9630071
[TBL] [Abstract][Full Text] [Related]
13. [Polymorphism of trinucleotide repeats at loci FRAXA and FRAXE in the population of Tomsk].
Tolmacheva EN; Nazarenko SA
Genetika; 2002 Feb; 38(2):268-73. PubMed ID: 11898618
[TBL] [Abstract][Full Text] [Related]
14. Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.
Liu T; Wang FS; Cheah FSH; Gu Y; Shaw M; Law HY; Tay SKH; Lee CG; Nelson DL; Gecz J; Chong SS
J Mol Diagn; 2021 Aug; 23(8):941-951. PubMed ID: 34111553
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
Nolin SL; Brown WT; Glicksman A; Houck GE; 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
Am J Hum Genet; 2003 Feb; 72(2):454-64. PubMed ID: 12529854
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an Indian population with mental retardation of unknown etiology.
Katikala L; Guruju MR; Madireddi S; Vallamkonda O; Vallamkonda N; Persha A; Spurgeon AM
Genet Test Mol Biomarkers; 2011 Apr; 15(4):281-4. PubMed ID: 21254876
[TBL] [Abstract][Full Text] [Related]
19. A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males.
Santos CB; Costa Lima MA; Pimentel MM
Hum Mutat; 2001 Aug; 18(2):157-62. PubMed ID: 11462240
[TBL] [Abstract][Full Text] [Related]
20. FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
Syrrou M; Georgiou I; Grigoriadou M; Petersen MB; Kitsiou S; Pagoulatos G; Patsalis PC
Genet Epidemiol; 1998; 15(1):103-9. PubMed ID: 9523214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
