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Items: 1 to 20 of 149

1.

Conflicts regarding genetic counseling for fragile X syndrome screening: a survey of clinical geneticists and genetic counselors in Israel.

Lieberman S, Zuckerman S, Levy-Lahad E, Altarescu G.

Am J Med Genet A. 2011 Sep;155A(9):2154-60. doi: 10.1002/ajmg.a.34155. Epub 2011 Aug 10.

PMID:
21834046
2.

Prenatal carrier testing for fragile X: counseling issues and challenges.

Musci TJ, Moyer K.

Obstet Gynecol Clin North Am. 2010 Mar;37(1):61-70, Table of Contents. doi: 10.1016/j.ogc.2010.03.004.

PMID:
20494258
3.

Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.

McConkie-Rosell A, Finucane B, Cronister A, Abrams L, Bennett RL, Pettersen BJ.

J Genet Couns. 2005 Aug;14(4):249-70.

PMID:
16047089
4.

Fragile X screening: attitudes of genetic health professionals.

Acharya K, Ross LF.

Am J Med Genet A. 2009 Feb 15;149A(4):626-32. doi: 10.1002/ajmg.a.32725.

5.

Attitudes toward prenatal screening and testing for Fragile X.

Fanos JH, Spangner KA, Musci TJ.

Genet Med. 2006 Feb;8(2):129-33.

PMID:
16481897
6.

Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

Toledano-Alhadef H, Basel-Vanagaite L, Magal N, Davidov B, Ehrlich S, Drasinover V, Taub E, Halpern GJ, Ginott N, Shohat M.

Am J Hum Genet. 2001 Aug;69(2):351-60. Epub 2001 Jul 6.

7.
8.

[Fragile X-associated tremor/ataxia syndrome].

Finke C, Horváth R, Holinski-Feder E, Ploner CJ.

Nervenarzt. 2009 Dec;80(12):1473-9. doi: 10.1007/s00115-009-2846-6. Review. German.

PMID:
19763529
9.

Attitudes toward fragile X mutation carrier testing from women identified in a general population survey.

Anido A, Carlson LM, Sherman SL.

J Genet Couns. 2007 Feb;16(1):97-104. Epub 2007 Feb 13.

PMID:
17295053
10.

[Family impact of FXTAS diagnosis: genetic counseling for at-risk relatives].

Lesca G, Lejeune S, Hernette D, Héron D.

Rev Neurol (Paris). 2013 Jun-Jul;169(6-7):515-8. doi: 10.1016/j.neurol.2012.12.005. Epub 2013 Apr 1. French.

PMID:
23557641
11.

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.

12.

"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant women.

Archibald AD, Jaques AM, Wake S, Collins VR, Cohen J, Metcalfe SA.

Am J Med Genet A. 2009 Dec;149A(12):2731-8. doi: 10.1002/ajmg.a.33122.

PMID:
19938084
13.

Provider biases and choices: the role of gender.

Wertz DC.

Clin Obstet Gynecol. 1993 Sep;36(3):521-31. Review.

PMID:
8403603
14.

Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.

Hiraki S, Ormond KE, Kim K, Ross LF.

Am J Med Genet A. 2006 Nov 1;140(21):2312-9.

PMID:
17036312
15.

Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses.

Xunclà M, Badenas C, Domínguez M, Rodríguez-Revenga L, Madrigal I, Jiménez L, Soler A, Borrell A, Sánchez A, Milà M.

Reprod Biomed Online. 2010 Oct;21(4):560-5. doi: 10.1016/j.rbmo.2010.05.015. Epub 2010 Jun 16.

PMID:
20801083
16.

A five-year experience with fragile X screening of high-risk gravid women.

Wenstrom KD, Descartes M, Franklin J, Cliver SP.

Am J Obstet Gynecol. 1999 Oct;181(4):789-92.

PMID:
10521730
17.

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
18.

Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.

Ryynänen M, Kirkinen P, Mannermaa A, Saarikoski S.

Am J Obstet Gynecol. 1995 Apr;172(4 Pt 1):1236-9.

PMID:
7726262
19.

ACOG Committee Opinion No. 469: Carrier screening for fragile X syndrome.

American College of Obstetricians and Gynecologists Committee on Genetics.

Obstet Gynecol. 2010 Oct;116(4):1008-10. doi: 10.1097/AOG.0b013e3181fae884.

PMID:
20859177
20.

[Screening for fragile X syndrome. International experiences].

Vuust J, Larsen LA, Grønskov K, Nørgaard-Pedersen B, Brøndum-Nielsen K.

Ugeskr Laeger. 2006 Oct 23;168(43):3704-9. Review. Danish.

PMID:
17069733
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