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.
148 related articles for article (PubMed ID: 8844099)
1. FRAXE mutation analysis in three Spanish families. Carbonell P; López I; Gabarrón J; Bernabé MJ; Lucas JM; Guitart M; Gabau E; Glover G Am J Med Genet; 1996 Aug; 64(2):434-40. PubMed ID: 8844099 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families. Russo S; Selicorni A; Bedeschi MF; Natacci F; Viziello P; Fortuna R; Pagani G; Dalprà L; Larizza L Am J Med Genet; 1998 Jan; 75(3):304-8. PubMed ID: 9475603 [TBL] [Abstract][Full Text] [Related]
5. Amplification of the Xq28 FRAXE repeats: extreme phenotype variability? Murgia A; Polli R; Vinanzi C; Salis M; Drigo P; Artifoni L; Zacchello F Am J Med Genet; 1996 Aug; 64(2):441-4. PubMed ID: 8844100 [TBL] [Abstract][Full Text] [Related]
6. 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]
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. A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs. Strelnikov V; Nemtsova M; Chesnokova G; Kuleshov N; Zaletayev D Hum Mutat; 1999; 13(2):166-9. PubMed ID: 10094554 [TBL] [Abstract][Full Text] [Related]
9. Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities. Holden JJ; Julien-Inalsingh C; Chalifoux M; Wing M; Scott E; Fidler K; Swift I; Maidment B; Knight SJ; Davies KE; White BN Am J Med Genet; 1996 Aug; 64(2):420-3. PubMed ID: 8844096 [TBL] [Abstract][Full Text] [Related]
10. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164 [TBL] [Abstract][Full Text] [Related]
11. FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother. Lo Nigro C; Faravelli F; Cavani S; Perroni L; Novello P; Vitali M; Bricarelli FD; Grasso M Eur J Hum Genet; 2000 Mar; 8(3):157-62. PubMed ID: 10780779 [TBL] [Abstract][Full Text] [Related]
12. A survey of fragile X syndrome in a sample from Spanish Basque country. Arrieta I; Criado B; Martinez B; Telez M; Nuñez T; Peñagarikano O; Ortega B; Lostao CM Ann Genet; 1999; 42(4):197-201. PubMed ID: 10674158 [TBL] [Abstract][Full Text] [Related]
13. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males. Biancalana V; Taine L; Bouix JC; Finck S; Chauvin A; De Verneuil H; Knight SJ; Stoll C; Lacombe D; Mandel JL Am J Hum Genet; 1996 Oct; 59(4):847-54. PubMed ID: 8808600 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardation. von Koskull H; Gahmberg N; Salonen R; Salo A; Peippo M Am J Med Genet; 1994 Jul; 51(4):486-9. PubMed ID: 7943025 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Clinical, cytogenetic, and molecular analysis of three families with FRAXE. Barnicoat AJ; Wang Q; Turk J; Green E; Mathew CG; Flynn G; Buckle V; Hirst M; Davies K; Bobrow M J Med Genet; 1997 Jan; 34(1):13-7. PubMed ID: 9032643 [TBL] [Abstract][Full Text] [Related]
19. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males. Soudek D; Partington MW; Lawson JS Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598 [TBL] [Abstract][Full Text] [Related]
20. The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers. Fishburn J; Turner G; Daniel A; Brookwell R Am J Med Genet; 1983 Apr; 14(4):713-24. PubMed ID: 6682625 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]