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Links from PubMed

Items: 12

1.

A complex mutable polymorphism located within the fragile X gene.

Zhong N, Dobkin C, Brown WT.

Nat Genet. 1993 Nov;5(3):248-53.

PMID:
8275089
2.

[Molecular and genetic features of fragile X syndrome].

Jara L, AvendaƱo I, Aspillaga M, Blanco R.

Rev Med Chil. 1996 Jul;124(7):865-72. Review. Spanish.

PMID:
9138377
3.

Fragile X syndrome.

Laxova R.

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

PMID:
7992687
4.
5.

Hypermethylation of telomere-like foldbacks at codon 12 of the human c-Ha-ras gene and the trinucleotide repeat of the FMR-1 gene of fragile X.

Smith SS, Laayoun A, Lingeman RG, Baker DJ, Riley J.

J Mol Biol. 1994 Oct 21;243(2):143-51. Review.

PMID:
7932745
6.

Human chromosome fragility.

Lukusa T, Fryns JP.

Biochim Biophys Acta. 2008 Jan;1779(1):3-16. Review.

PMID:
18078840
7.

Significance of linkage disequilibrium between the fragile X locus and its flanking markers.

Chiurazzi P, Macpherson J, Sherman S, Neri G.

Am J Med Genet. 1996 Jul 12;64(1):203-8. Review. No abstract available.

PMID:
8826477
8.

Unusual inheritance patterns due to dynamic mutation in fragile X syndrome.

Sutherland GR, Richards RI.

Ciba Found Symp. 1996;197:119-26; discussion 126-36. Review.

PMID:
8827371
9.

An assessment of screening strategies for fragile X syndrome in the UK.

Pembrey ME, Barnicoat AJ, Carmichael B, Bobrow M, Turner G.

Health Technol Assess. 2001;5(7):1-95. Review.

10.

The unstable and methylatable mutations causing the fragile X syndrome.

Rousseau F, Heitz D, Mandel JL.

Hum Mutat. 1992;1(2):91-6. Review. No abstract available.

PMID:
1301206
11.

Dynamic mutations: a new class of mutations causing human disease.

Richards RI, Sutherland GR.

Cell. 1992 Sep 4;70(5):709-12. Review. No abstract available.

PMID:
1516128
12.

Triplet repeat expansion mutations: the example of fragile X syndrome.

Warren ST, Ashley CT Jr.

Annu Rev Neurosci. 1995;18:77-99. Review. No abstract available.

PMID:
7605075
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