These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 20548240)

  • 1. 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. PubMed ID: 20548240
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Attitudes toward prenatal screening and testing for Fragile X.
    Fanos JH; Spangner KA; Musci TJ
    Genet Med; 2006 Feb; 8(2):129-33. PubMed ID: 16481897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Commentary on population screening for fragile X syndrome.
    Coffee B
    Genet Med; 2010 Jul; 12(7):411-2. PubMed ID: 20535018
    [No Abstract]   [Full Text] [Related]  

  • 4. "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. PubMed ID: 19938084
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Screening for fragile X syndrome. International experiences].
    Vuust J; Larsen LA; Grønskov K; Nørgaard-Pedersen B; Brøndum-Nielsen K
    Ugeskr Laeger; 2006 Oct; 168(43):3704-9. PubMed ID: 17069733
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 11262423
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 20494258
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Newborn screening for fragile X syndrome.
    Bailey DB
    Ment Retard Dev Disabil Res Rev; 2004; 10(1):3-10. PubMed ID: 14994282
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fragile X syndrome detection in newborns-pilot study.
    Saul RA; Friez M; Eaves K; Stapleton GA; Collins JS; Schwartz CE; Stevenson RE
    Genet Med; 2008 Oct; 10(10):714-9. PubMed ID: 18813135
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening for fragile X syndrome.
    Murray J; Cuckle H; Taylor G; Hewison J
    Health Technol Assess; 1997; 1(4):i-iv, 1-71. PubMed ID: 9414543
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fragile X screening: attitudes of genetic health professionals.
    Acharya K; Ross LF
    Am J Med Genet A; 2009 Feb; 149A(4):626-32. PubMed ID: 19291766
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Attitudes toward population screening among people living with fragile X syndrome in the UK: 'I wouldn't wish him away, I'd just wish his fragile X syndrome away'.
    Boardman FK
    J Genet Couns; 2021 Feb; 30(1):85-97. PubMed ID: 33184995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.
    Bailey DB; Skinner D; Davis AM; Whitmarsh I; Powell C
    Pediatrics; 2008 Mar; 121(3):e693-704. PubMed ID: 18310190
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome.
    Godler DE; Slater HR; Amor D; Loesch DZ
    Genet Med; 2010 Sep; 12(9):595. PubMed ID: 20838083
    [No Abstract]   [Full Text] [Related]  

  • 15. Fragile X testing in obstetrics and gynaecology in Canada.
    Chitayat D; Wyatt PR; ;
    J Obstet Gynaecol Can; 2008 Sep; 30(9):837-841. PubMed ID: 18845054
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for fragile X syndrome in women of reproductive age.
    Pesso R; Berkenstadt M; Cuckle H; Gak E; Peleg L; Frydman M; Barkai G
    Prenat Diagn; 2000 Aug; 20(8):611-4. PubMed ID: 10951469
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Challenges in prenatal screening and counselling for fragile X syndrome.
    Mak AS; Leung KY
    Hong Kong Med J; 2017 Apr; 23(2):108-9. PubMed ID: 28387201
    [No Abstract]   [Full Text] [Related]  

  • 18. Maternal attitudes to newborn screening for fragile X syndrome.
    Christie L; Wotton T; Bennetts B; Wiley V; Wilcken B; Rogers C; Boyle J; Turner C; Hansen J; Hunter M; Goel H; Field M
    Am J Med Genet A; 2013 Feb; 161A(2):301-11. PubMed ID: 23303663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Economic evaluation of prenatal population screening for fragile X syndrome.
    Hollingsworth B; Harris A
    Community Genet; 2005; 8(2):68-72. PubMed ID: 15925881
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 16047089
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.