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Results: 19

Related Articles by Review for PubMed (Select 18941415)

1.

Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines.

Kronquist KE, Sherman SL, Spector EB.

Genet Med. 2008 Nov;10(11):845-7. doi: 10.1097/GIM.0b013e31818b0c8a. No abstract available.

2.

Fragile X and other trinucleotide repeat diseases.

Wenstrom KD.

Obstet Gynecol Clin North Am. 2002 Jun;29(2):367-88, vii. Review.

PMID:
12108834
3.

The fragile X syndrome and other fragile site disorders.

Kooy RF, Oostra BA, Willems PJ.

Results Probl Cell Differ. 1998;21:1-46. Review. No abstract available.

PMID:
9670313
4.

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
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.

Fragile X syndrome in humans and mice.

Oostra BA.

Acta Genet Med Gemellol (Roma). 1996;45(1-2):93-108. Review. No abstract available.

PMID:
8872018
7.

Fragile X syndrome at the turn of the century.

Kooy RF, Willemsen R, Oostra BA.

Mol Med Today. 2000 May;6(5):193-8. Review.

PMID:
10782066
8.

Understanding the molecular basis of fragile X syndrome.

Jin P, Warren ST.

Hum Mol Genet. 2000 Apr 12;9(6):901-8. Review.

9.

FMR1 and the fragile X syndrome: human genome epidemiology review.

Crawford DC, Acuña JM, Sherman SL.

Genet Med. 2001 Sep-Oct;3(5):359-71. Review.

PMID:
11545690
10.

[Molecular cytogenetics of fragile X syndrome].

Yamauchi M, Tsuji S, Hori T.

Nihon Rinsho. 1999 Apr;57(4):943-9. Review. Japanese.

PMID:
10222794
11.

[Medical pathology due to trinucleotide repeats].

Arenas-Aranda D, Peñaloza R, Salamanca-Gómez F.

Gac Med Mex. 1999 Jan-Feb;135(1):53-65. Review. Spanish.

PMID:
10204311
12.

[The role of trinucleotide repeats in human genetic diseases].

Hietanen K.

Duodecim. 1996;112(3):188-93. Review. Finnish. No abstract available.

PMID:
10590627
13.

Molecular diagnosis of inherited diseases.

Murgia A, Polli R, Martella M, Vinanzi C, Opocher G.

Clin Chim Acta. 1999 Feb;280(1-2):73-80. Review. Erratum in: Clin Chim Acta 1999 Apr;28(1-2):229. Murigia A [corrected to Murgia A].

PMID:
10090525
14.

Fragile X syndrome (review).

Pimentel MM.

Int J Mol Med. 1999 Jun;3(6):639-45. Review.

PMID:
10341296
15.

Fragile X-associated tremor/ataxia syndrome (FXTAS).

Hagerman PJ, Hagerman RJ.

Ment Retard Dev Disabil Res Rev. 2004;10(1):25-30. Review.

PMID:
14994285
16.

[Fragile X syndrome].

Arinami T.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):358-60. Review. Japanese. No abstract available.

PMID:
11057260
17.

RNA and microRNAs in fragile X mental retardation.

Jin P, Alisch RS, Warren ST.

Nat Cell Biol. 2004 Nov;6(11):1048-53. Review.

PMID:
15516998
18.

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
19.

[Diagnostic testing in fragile X syndrome].

Sireteanu A, Rusu C.

Rev Med Chir Soc Med Nat Iasi. 2006 Oct-Dec;110(4):968-71. Review. Romanian.

PMID:
17438909
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