200 related articles for article (PubMed ID: 8062436)
1. Fragile X syndrome with extra microchromosome.
López-Pajares I; Delicado A; Pascual-Castroviejo I; López-Martin V; Moreno F; Garcia-Marcos JA
Clin Genet; 1994 Apr; 45(4):186-9. PubMed ID: 8062436
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.
Butler MG; Pratesi R; Vnencak-Jones CL
J Intellect Disabil Res; 1995 Dec; 39 ( Pt 6)(Pt 6):544-53. PubMed ID: 8746743
[TBL] [Abstract][Full Text] [Related]
3. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
Proops R; Webb T
J Med Genet; 1981 Oct; 18(5):366-73. PubMed ID: 7328617
[TBL] [Abstract][Full Text] [Related]
4. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome.
Li SY; Tsai CC; Chou MY; Lin JK
Hum Genet; 1988 Aug; 79(4):292-6. PubMed ID: 2970423
[TBL] [Abstract][Full Text] [Related]
5. Cytogenetically negative, linkage positive "fragile X" syndrome.
Sklower Brooks S; Cohen I; Ferrando C; Jenkins EC; Brown WT; Dobkin C
Am J Med Genet; 1991; 38(2-3):370-3. PubMed ID: 1673313
[TBL] [Abstract][Full Text] [Related]
6. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
Oberlé I; Boué J; Croquette MF; Voelckel MA; Mattei MG; Mandel JL
Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):224-31. PubMed ID: 1605195
[TBL] [Abstract][Full Text] [Related]
7. Is there a fragile(X) negative Martin-Bell syndrome?
Thode A; Laing S; Partington MW; Turner G
Am J Med Genet; 1988; 30(1-2):459-71. PubMed ID: 3052069
[TBL] [Abstract][Full Text] [Related]
8. [The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes].
Giné R; Espinás ML; Antich J; Carballo M
Med Clin (Barc); 1992 Feb; 98(4):121-4. PubMed ID: 1552760
[TBL] [Abstract][Full Text] [Related]
9. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
[TBL] [Abstract][Full Text] [Related]
10. Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.
Butler MG; Singh DN
J Intellect Disabil Res; 1993 Apr; 37 ( Pt 2)(Pt 2):131-42. PubMed ID: 8481611
[TBL] [Abstract][Full Text] [Related]
11. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.
Arinami T; Kondo I; Nakajima S; Hamaguchi H
Hum Genet; 1987 Aug; 76(4):344-7. PubMed ID: 3610153
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.
Butler MG; Allen GA; Haynes JL; Clark SJ
Am J Med Genet; 1990 Oct; 37(2):250-3. PubMed ID: 2248293
[TBL] [Abstract][Full Text] [Related]
14. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
Haspeslagh M; Fryns JP; Holvoet M; Collen G; Dierck G; Baeke J; van den Berghe H
Clin Genet; 1991 Jun; 39(6):434-41. PubMed ID: 1863991
[TBL] [Abstract][Full Text] [Related]
15. The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986.
Veenema H; Beverstock GC; de Koning T; Pearson PL; van de Kamp JJ
Clin Genet; 1988 Jun; 33(6):410-7. PubMed ID: 3168313
[TBL] [Abstract][Full Text] [Related]
16. Fragile site X chromosomes in mentally retarded boys.
Moon HR; Moon SY
J Korean Med Sci; 1993 Jun; 8(3):192-6. PubMed ID: 8240748
[TBL] [Abstract][Full Text] [Related]
17. [The fragile X chromosome syndrome: DNA analysis in families with familial occurrence of mental retardation].
Poláková H; Khoury L; Cierna M
Bratisl Lek Listy; 1997 Mar; 98(3):150-6. PubMed ID: 9264820
[TBL] [Abstract][Full Text] [Related]
18. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
[TBL] [Abstract][Full Text] [Related]
19. Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece.
Mavrou A; Syrrou M; Tsenghi C; Metaxotou C
Am J Med Genet; 1991; 38(2-3):437-9. PubMed ID: 2018086
[TBL] [Abstract][Full Text] [Related]
20. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
Schinzel A; Largo RH
Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
