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Results: 1 to 20 of 28

1.

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.

Bell MV, Hirst MC, Nakahori Y, MacKinnon RN, Roche A, Flint TJ, Jacobs PA, Tommerup N, Tranebjaerg L, Froster-Iskenius U, et al.

Cell. 1991 Feb 22;64(4):861-6.

PMID:
1997211
[PubMed - indexed for MEDLINE]
2.

DNA studies of X-linked mental retardation associated with a fragile site at Xq27.

Davies KE.

Am J Med Genet. 1986 Jan-Feb;23(1-2):633-42. Review.

PMID:
3513572
[PubMed - indexed for MEDLINE]
3.

[The diagnosis of mental retardation in fragile X syndrome is revolutionized by molecular genetics].

Lemire M, Rousseau F.

Union Med Can. 1993 Jan-Feb;122(1):23-9. Review. French.

PMID:
8465472
[PubMed - indexed for MEDLINE]
4.

Fragile X-linked mental retardation and the difficulties of reverse genetics.

Jordan BR.

Bioessays. 1991 May;13(5):243-51. Review.

PMID:
1679986
[PubMed - indexed for MEDLINE]
5.

[Fragile X syndrome: current knowledge].

Pellissier MC, Voelckel MA, Mattei JF.

Pediatrie. 1992;47(11):743-50. Review. French.

PMID:
1364151
[PubMed - indexed for MEDLINE]
6.

Fragile X syndrome.

Laxova R.

Adv Pediatr. 1994;41:305-42. Review.

PMID:
7992687
[PubMed - indexed for MEDLINE]
7.

Non-specific X-linked mental retardation: background, types, diagnosis and prevalence.

Howard-Peebles PN.

J Ment Defic Res. 1982 Dec;26 (Pt 4):205-13. Review.

PMID:
6763078
[PubMed - indexed for MEDLINE]
8.

Fragile X syndrome and fragile XE mental retardation.

Sutherland GR, Mulley JC.

Prenat Diagn. 1996 Dec;16(13):1199-211. Review.

PMID:
9061751
[PubMed - indexed for MEDLINE]
9.

Fragile X syndrome: a major cause of X-linked mental retardation.

Butler MG.

Compr Ther. 1988 Jul;14(7):3-7. Review. No abstract available.

PMID:
3060303
[PubMed - indexed for MEDLINE]
10.

[Mental retardation linked to fragility of chromosome X: current knowledge].

Mattei JF, Mattei MG, Auger M, Giraud F.

J Genet Hum. 1984 Jul;32(3):167-92. Review. French.

PMID:
6237176
[PubMed - indexed for MEDLINE]
11.

Molecular genetic advances in fragile X syndrome.

Tarleton JC, Saul RA.

J Pediatr. 1993 Feb;122(2):169-85. Review.

PMID:
8429429
[PubMed - indexed for MEDLINE]
12.

The fragile-X syndrome: a growing gene causing familial intellectual disability.

De Vries LB, Halley DJ, Oostra BA, Niermeijer MF.

J Intellect Disabil Res. 1994 Feb;38 ( Pt 1):1-8. Review.

PMID:
8173220
[PubMed - indexed for MEDLINE]
13.

[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome].

Tizzano Ferrari E, Gallano Petit P, Baiget Bastus M.

An Esp Pediatr. 1992 Apr;36(4):272-6. Review. Spanish.

PMID:
1605409
[PubMed - indexed for MEDLINE]
14.

[The clinico-genetic aspects of mental retardation related to the fragile-X chromosome].

Viekhova NV, Demydova IA, Bychkova HM, Vorsanova SH, Buzhiievs'ka TI.

Tsitol Genet. 1992 Nov-Dec;26(6):64-71. Review. Ukrainian.

PMID:
1292164
[PubMed - indexed for MEDLINE]
15.

The fragile X syndrome.

Brown WT.

Neurol Clin. 1989 Feb;7(1):107-21. Review.

PMID:
2646518
[PubMed - indexed for MEDLINE]
16.

The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects.

Gecz J.

Ann Hum Genet. 2000 Mar;64(Pt 2):95-106. Review.

PMID:
11246464
[PubMed - indexed for MEDLINE]
17.

Genetics and expression of the fragile X syndrome.

Brown WT, Jenkins EC, Gross AC, Chan CB, Wisniewski K, Cohen IL, Miezejeski CM.

Ups J Med Sci Suppl. 1987;44:137-54. Review.

PMID:
2895523
[PubMed - indexed for MEDLINE]
18.

[X-linked mental retardation without fragile X chromosome].

Piussan C.

Arch Fr Pediatr. 1990 Dec;47(10):701-3. Review. French. No abstract available.

PMID:
2082841
[PubMed - indexed for MEDLINE]
19.

Molecular genetics of the human X chromosome.

Davies KE.

J Med Genet. 1985 Aug;22(4):243-9. Review.

PMID:
2995673
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

[Martin-Bell syndrome (mental retardation with fragile X syndrome (review of the literature)].

Kuprianova TA.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1991;91(8):115-25. Review. Russian. No abstract available.

PMID:
1661501
[PubMed - indexed for MEDLINE]

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