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Results: 1 to 20 of 84

Similar articles for PubMed (Select 23687552)

1.

Prenatal screening for fragile x: carriers, controversies, and counseling.

Gutiérrez JF, Bajaj K, Klugman SD.

Rev Obstet Gynecol. 2013;6(1):e1-7.

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.

Prenatal diagnosis and carrier screening for fragile X by PCR.

Brown WT, Nolin S, Houck G Jr, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E.

Am J Med Genet. 1996 Jul 12;64(1):191-5.

PMID:
8826474
4.

The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families.

Geva E, Yaron Y, Shomrat R, Ben-Yehuda A, Zabari S, Peretz H, Naiman T, Yeger H, Orr-Urtreger A.

Genet Test. 2000;4(3):289-92.

PMID:
11142761
5.

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.

6.

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.

7.

Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.

Finucane B, Abrams L, Cronister A, Archibald AD, Bennett RL, McConkie-Rosell A.

J Genet Couns. 2012 Dec;21(6):752-60. doi: 10.1007/s10897-012-9524-8. Epub 2012 Jul 14. Erratum in: J Genet Couns. 2012 Dec;21(6):985.

PMID:
22797890
8.

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
9.

Newborn, carrier, and early childhood screening recommendations for fragile X.

Abrams L, Cronister A, Brown WT, Tassone F, Sherman SL, Finucane B, McConkie-Rosell A, Hagerman R, Kaufmann WE, Picker J, Coffey S, Skinner D, Johnson V, Miller R, Berry-Kravis E.

Pediatrics. 2012 Dec;130(6):1126-35. doi: 10.1542/peds.2012-0693. Epub 2012 Nov 5. Review.

10.

Fragile X syndrome carrier screening in the prenatal genetic counseling setting.

Cronister A, DiMaio M, Mahoney MJ, Donnenfeld AE, Hallam S.

Genet Med. 2005 Apr;7(4):246-50.

PMID:
15834242
11.

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
12.

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
13.

Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia.

Martorell L, Tondo M, Garcia-Fructuoso F, Naudo M, Alegre C, Gamez J, Genovés J, Poo P.

Clin Rheumatol. 2012 Nov;31(11):1611-5. doi: 10.1007/s10067-012-2052-y. Epub 2012 Aug 18.

PMID:
22903700
14.

Fragile-X syndrome in east Finland: molecular approach to genetic and prenatal diagnosis.

Ryynänen M, Pulkkinen L, Kirkinen P, Saarikoski S.

Am J Med Genet. 1994 Jul 15;51(4):463-5.

PMID:
7943020
15.

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
16.

DNA testing for fragile X syndrome in schools for learning difficulties.

Slaney SF, Wilkie AO, Hirst MC, Charlton R, McKinley M, Pointon J, Christodoulou Z, Huson SM, Davies KE.

Arch Dis Child. 1995 Jan;72(1):33-7.

17.

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.

18.

Checklist assessments of FMR1 gene mutation phenotypes.

Johnson VA.

J Cult Divers. 2008 Fall;15(3):117-31. Review.

PMID:
19025200
19.

Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies.

Ryynänen M, Heinonen S, Makkonen M, Kajanoja E, Mannermaa A, Pertti K.

Eur J Hum Genet. 1999 Feb-Mar;7(2):212-6.

20.

[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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