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Results: 17

Related Articles by Review for PubMed (Select 7849707)

1.

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ.

Hum Mol Genet. 1994 Oct;3(10):1823-7.

PMID:
7849707
2.

Fragile X syndrome and deletions in FMR1: new case and review of the literature.

Hammond LS, Macias MM, Tarleton JC, Shashidhar Pai G.

Am J Med Genet. 1997 Nov 12;72(4):430-4. Review.

PMID:
9375726
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. Review.

PMID:
15135801
4.

A fragile gene.

Oostra BA, Willems PJ.

Bioessays. 1995 Nov;17(11):941-7. Review.

PMID:
8526888
5.

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.

6.

Severe mental retardation and macroorchidism without mutation in the FMR1 gene.

Reyniers E, Wolff G, Tariverdian G, De Boulle K, Storm K, Kooy RF, Willems PJ.

Am J Med Genet. 1996 Aug 9;64(2):408-12. Review.

PMID:
8844093
7.

A fragile balance: FMR1 expression levels.

Oostra BA, Willemsen R.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R249-57. Epub 2003 Sep 2. Review.

8.

Molecular diagnosis and genetic counseling for fragile X mental retardation.

Pandey UB, Phadke SR, Mittal B.

Neurol India. 2004 Mar;52(1):36-42. Review.

9.

Molecular analysis of the fragile X syndrome.

Knight SJ, Hirst MC, Davies KE.

Dis Markers. 1992 Jan-Feb;10(1):1-5. Review.

PMID:
1424438
10.

The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation.

Oostra BA, Verkerk AJ.

Chromosoma. 1992 Apr;101(7):381-7. Review.

PMID:
1618021
11.

Complex behavior of simple repeats: the fragile X syndrome.

Oostra BA, Halley DJ.

Pediatr Res. 1995 Nov;38(5):629-37. Review.

PMID:
8552426
12.

Advances in molecular analysis of fragile X syndrome.

Warren ST, Nelson DL.

JAMA. 1994 Feb 16;271(7):536-42. Review.

PMID:
8301769
13.

The fragile X syndromes.

Nelson DL.

Semin Cell Biol. 1995 Feb;6(1):5-11. Review.

PMID:
7620122
14.

The fragile X syndrome.

Flannery AV, Hirst MC, Knight SJ, Ritchie RJ, Davies KE.

Biochim Biophys Acta. 1995 Jun 9;1271(2-3):293-303. Review. No abstract available.

PMID:
7605796
15.

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
16.

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
17.

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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