377 related articles for article (PubMed ID: 18712171)
1. 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
Sofocleous C; Kitsiou S; Fryssira H; Kolialexi A; Kalaitzidaki M; Roma E; Tsangaris GT; Chistofidou C; Metaxotou C; Kanavakis E; Mavrou A
In Vivo; 2008; 22(4):451-5. PubMed ID: 18712171
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Clinical and molecular screening for fragile X syndrome in 300 patients with non-specific mental retardation].
Jara L; López M; Mellado C; Aspillaga M; Avendaño I; Blanco R
Rev Med Chil; 1998 Aug; 126(8):911-8. PubMed ID: 9830742
[TBL] [Abstract][Full Text] [Related]
5. [A genetic and molecular study of 85 families affected with the fragile X syndrome].
Milà Recasens M; Sánchez Díaz A; Glover López G; Castellví Bel S; Carbonell Meseguer P; Kruyer H; Ballesta Martínez F; Estivill Pallejà X
An Esp Pediatr; 1996 Mar; 44(3):250-6. PubMed ID: 8830601
[TBL] [Abstract][Full Text] [Related]
6. [X-linked mental retardation: variations in the fragile X mutations and genetic counseling].
Kondo I; Kurokawa Y
Nihon Koshu Eisei Zasshi; 1993 Aug; 40(8):599-605. PubMed ID: 8219287
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Prenatal diagnosis and carrier screening for fragile X by PCR.
Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Stark-Houck S; Brophy P; Duncan C; Dobkin C; Jenkins E
Am J Med Genet; 1996 Jul; 64(1):191-5. PubMed ID: 8826474
[TBL] [Abstract][Full Text] [Related]
9. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.
Lachiewicz AM; Spiridigliozzi GA; McConkie-Rosell A; Burgess D; Feng Y; Warren ST; Tarleton J
Am J Med Genet; 1996 Aug; 64(2):278-82. PubMed ID: 8844065
[TBL] [Abstract][Full Text] [Related]
10. Molecular screening for fragile X syndrome in Thailand.
Limprasert P; Ruangdaraganon N; Sura T; Vasiknanonte P; Jinorose U
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():114-8. PubMed ID: 11400746
[TBL] [Abstract][Full Text] [Related]
11. Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.
Pouya AR; Abedini SS; Mansoorian N; Behjati F; Nikzat N; Mohseni M; Nieh SE; Abbasi Moheb L; Darvish H; Monajemi GB; Banihashemi S; Kahrizi K; Ropers HH; Najmabadi H
Eur J Med Genet; 2009; 52(4):170-3. PubMed ID: 19361583
[TBL] [Abstract][Full Text] [Related]
12. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
[TBL] [Abstract][Full Text] [Related]
13. [From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene].
de Vries LB; Oostra BA
Ned Tijdschr Geneeskd; 2001 Mar; 145(10):474-6. PubMed ID: 11268909
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
[TBL] [Abstract][Full Text] [Related]
17. Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients.
Pang CP; Poon PM; Chen QL; Lai KY; Yin CH; Zhao Z; Zhong N; Lau CH; Lam ST; Wong CK; Brown WT
Am J Med Genet; 1999 May; 84(3):179-83. PubMed ID: 10331586
[TBL] [Abstract][Full Text] [Related]
18. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; Constantinou-Deltas CD; Pagoulatos G
Am J Med Genet; 1996 Jul; 64(1):234-8. PubMed ID: 8826482
[TBL] [Abstract][Full Text] [Related]
19. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
[TBL] [Abstract][Full Text] [Related]
20. DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.
van den Ouweland AM; de Vries BB; Bakker PL; Deelen WH; de Graaff E; van Hemel JO; Oostra BA; Niermeijer MF; Halley DJ
Am J Med Genet; 1994 Jul; 51(4):482-5. PubMed ID: 7943024
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]