BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 21853527)

  • 1. A majority of parents accept newborn screening for fragile X.
    Levenson D
    Am J Med Genet A; 2011 Sep; 155A(9):viii-ix. PubMed ID: 21853527
    [No Abstract]   [Full Text] [Related]  

  • 2. Molloy v Meier and the expanding standard of medical care: implications for public health policy and practice.
    Burke T; Rosenbaum S
    Public Health Rep; 2005; 120(2):209-10. PubMed ID: 15842124
    [No Abstract]   [Full Text] [Related]  

  • 3. Screening for Fragile X Syndrome: parent attitudes and perspectives.
    Skinner D; Sparkman KL; Bailey DB
    Genet Med; 2003; 5(5):378-84. PubMed ID: 14501833
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X Newborn Screening: Lessons Learned From a Multisite Screening Study.
    Bailey DB; Berry-Kravis E; Gane LW; Guarda S; Hagerman R; Powell CM; Tassone F; Wheeler A
    Pediatrics; 2017 Jun; 139(Suppl 3):S216-S225. PubMed ID: 28814542
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Testing for fragile X gene mutations throughout the life span.
    Hagerman RJ; Hagerman PJ
    JAMA; 2008 Nov; 300(20):2419-21. PubMed ID: 19033593
    [No Abstract]   [Full Text] [Related]  

  • 8. Newborn screening for fragile x syndrome: do we care what parents think?
    Botkin JR
    Pediatrics; 2011 Jun; 127(6):e1593-4. PubMed ID: 21624877
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. [A large-scale diagnostic program for the fragile X-syndrome among the mentally retarded. II. Implications for parents and family].
    de Vries LB; Duivenvoorden HJ; Tibben A; Niermeijer MF
    Ned Tijdschr Geneeskd; 1998 Jul; 142(29):1672-5. PubMed ID: 9890807
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ethical and policy issues in newborn screening of children for neurologic and developmental disorders.
    Ross LF
    Pediatr Clin North Am; 2015 Jun; 62(3):787-98. PubMed ID: 26022175
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 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. Fragile X syndrome.
    Welch JL; Williams JK
    Neonatal Netw; 1999 Sep; 18(6):15-22. PubMed ID: 10690095
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.
    Skinner D; Choudhury S; Sideris J; Guarda S; Buansi A; Roche M; Powell C; Bailey DB
    Pediatrics; 2011 Jun; 127(6):e1455-63. PubMed ID: 21624881
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Pilot Study of Fragile X Syndrome Screening in Pregnant Women and Women Planning Pregnancy: Implementation, Acceptance, Awareness, and Geographic Factors.
    Alfaro Arenas R; Rosell Andreo J; Heine Suñer D;
    J Genet Couns; 2017 Jun; 26(3):501-510. PubMed ID: 27714485
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Policy considerations in designing a fragile X population screening program.
    Ross LF; Acharya K
    Genet Med; 2008 Oct; 10(10):711-3. PubMed ID: 18813132
    [No Abstract]   [Full Text] [Related]  

  • 20. Methylation analysis in newborn screening for fragile X syndrome.
    Godler DE; Amor DJ; Slater HR
    JAMA Neurol; 2014 Jun; 71(6):800. PubMed ID: 24911126
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.