96 related articles for article (PubMed ID: 1303227)
1. Clinical conundrums in fragile X syndrome.
Hagerman R
Nat Genet; 1992 Jun; 1(3):157-8. PubMed ID: 1303227
[No Abstract] [Full Text] [Related]
2. 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]
3. Neurobiology of Fragile X syndrome: from molecular genetics to neurobehavioral phenotype.
Kaufmann WE
Microsc Res Tech; 2002 May; 57(3):131-4. PubMed ID: 12112447
[No Abstract] [Full Text] [Related]
4. [Last advances in Fragile X chromosome syndrome].
Bañares VG
Medicina (B Aires); 1995; 55(5 Pt 1):457-66. PubMed ID: 8728777
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A point mutation in the FMR-1 gene associated with fragile X mental retardation.
De Boulle K; Verkerk AJ; Reyniers E; Vits L; Hendrickx J; Van Roy B; Van den Bos F; de Graaff E; Oostra BA; Willems PJ
Nat Genet; 1993 Jan; 3(1):31-5. PubMed ID: 8490650
[TBL] [Abstract][Full Text] [Related]
7. Transgenic mouse model for the fragile X syndrome.
Kooy RF; D'Hooge R; Reyniers E; Bakker CE; Nagels G; De Boulle K; Storm K; Clincke G; De Deyn PP; Oostra BA; Willems PJ
Am J Med Genet; 1996 Aug; 64(2):241-5. PubMed ID: 8844056
[TBL] [Abstract][Full Text] [Related]
8. Huntington's disease: testing the test.
Read AP
Nat Genet; 1993 Aug; 4(4):329-30. PubMed ID: 8401575
[No Abstract] [Full Text] [Related]
9. Enhanced Fmr-1 expression in testis.
Bächner D; Stéinbach P; Wöhrle D; Just W; Vogel W; Hameister H; Manca A; Poustka A
Nat Genet; 1993 Jun; 4(2):115-6. PubMed ID: 8348147
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling.
Fryns JP; Curfs LM; Cassiman JJ; van den Berghe H
Genet Couns; 1992; 3(4):175-7. PubMed ID: 1361752
[No Abstract] [Full Text] [Related]
13. [Mental retardation and fragile X syndrome].
Nanba E
No To Shinkei; 1998 Apr; 50(4):317-23. PubMed ID: 9592820
[No Abstract] [Full Text] [Related]
14. Transmitting males and carrier females in fragile X--revisited.
Loesch DZ; Hay DA; Mulley J
Am J Med Genet; 1994 Jul; 51(4):392-9. PubMed ID: 7943005
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of the fragile X syndrome.
Knight SJ; Hirst MC; Davies KE
Dis Markers; 1992; 10(1):1-5. PubMed ID: 1424438
[TBL] [Abstract][Full Text] [Related]
16. Dilemmas in counselling females with the fragile X syndrome.
de Vries BB; van den Boer-van den Berg HM; Niermeijer MF; Tibben A
J Med Genet; 1999 Feb; 36(2):167-70. PubMed ID: 10051021
[TBL] [Abstract][Full Text] [Related]
17. Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.
Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJ; Horst J; Mazurczak T
Acta Biochim Pol; 1996; 43(2):383-8. PubMed ID: 8862184
[TBL] [Abstract][Full Text] [Related]
18. A new regulatory pathway for fragile X syndrome?
Hansen RS; Laird CD
Nat Med; 2002 Nov; 8(11):1204-5. PubMed ID: 12411943
[No Abstract] [Full Text] [Related]
19. Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene.
Fryns JP; D'Hooghe M; Devriendt K
Genet Couns; 1996; 7(3):227-30. PubMed ID: 8897045
[TBL] [Abstract][Full Text] [Related]
20. DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature.
Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; Morel ML; Rousseau F
Am J Med Genet; 1999 Apr; 83(4):347-9. PubMed ID: 10208178
[No Abstract] [Full Text] [Related]
[Next] [New Search]
