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Items: 16

1.

Fragile X analysis of 1112 prenatal samples from 1991 to 2010.

Nolin SL, Glicksman A, Ding X, Ersalesi N, Brown WT, Sherman SL, Dobkin C.

Prenat Diagn. 2011 Oct;31(10):925-31. doi: 10.1002/pd.2815. Epub 2011 Jun 30.

PMID:
21717484
2.

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.

3.

The fragile X premutation: into the phenotypic fold.

Hagerman RJ, Hagerman PJ.

Curr Opin Genet Dev. 2002 Jun;12(3):278-83. Review.

PMID:
12076670
4.

The Fragile X premutation: new insights and clinical consequences.

Van Esch H.

Eur J Med Genet. 2006 Jan-Feb;49(1):1-8. Epub 2005 Dec 5. Review.

PMID:
16473304
5.

The FMR1 premutation and reproduction.

Wittenberger MD, Hagerman RJ, Sherman SL, McConkie-Rosell A, Welt CK, Rebar RW, Corrigan EC, Simpson JL, Nelson LM.

Fertil Steril. 2007 Mar;87(3):456-65. Epub 2006 Oct 30. Review.

PMID:
17074338
6.

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.

7.

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.

Rajan-Babu IS, Lian M, Cheah FSH, Chen M, Tan ASC, Prasath EB, Loh SF, Chong SS.

Expert Rev Mol Med. 2017 Jul 19;19:e10. doi: 10.1017/erm.2017.10. Review.

8.

Advanced technologies for the molecular diagnosis of fragile X syndrome.

Tassone F.

Expert Rev Mol Diagn. 2015;15(11):1465-73. doi: 10.1586/14737159.2015.1101348. Epub 2015 Oct 21. Review.

9.

Fragile X-associated disorders: a clinical overview.

Gallagher A, Hallahan B.

J Neurol. 2012 Mar;259(3):401-13. doi: 10.1007/s00415-011-6161-3. Epub 2011 Jul 12. Review.

PMID:
21748281
10.

Fragile X syndrome.

Saldarriaga W, Tassone F, González-Teshima LY, Forero-Forero JV, Ayala-Zapata S, Hagerman R.

Colomb Med (Cali). 2014 Dec 30;45(4):190-8. eCollection 2014 Oct-Dec. Review.

11.

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.

Hunter J, Rivero-Arias O, Angelov A, Kim E, Fotheringham I, Leal J.

Am J Med Genet A. 2014 Jul;164A(7):1648-58. doi: 10.1002/ajmg.a.36511. Epub 2014 Apr 3. Review.

PMID:
24700618
12.

[Genetics of Fragile X syndrome and its prevention].

Boué J, Simon-Bouy B.

J Gynecol Obstet Biol Reprod (Paris). 1997;26(3):273-9. Review. French.

PMID:
9265049
13.

Newborn screening for fragile X syndrome.

Tassone F.

JAMA Neurol. 2014 Mar;71(3):355-9. doi: 10.1001/jamaneurol.2013.4808. Review.

14.

A systematic review of population screening for fragile X syndrome.

Hill MK, Archibald AD, Cohen J, Metcalfe SA.

Genet Med. 2010 Jul;12(7):396-410. doi: 10.1097/GIM.0b013e3181e38fb6. Review.

PMID:
20548240
15.

Screening for fragile X syndrome: information needs for health planners.

Murray J, Cuckle H, Taylor G, Hewison J.

J Med Screen. 1997;4(2):60-94. Review. No abstract available.

PMID:
9275266
16.

The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.

Latham GJ, Coppinger J, Hadd AG, Nolin SL.

Front Genet. 2014 Jul 29;5:244. doi: 10.3389/fgene.2014.00244. eCollection 2014. Review.

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