156 related articles for article (PubMed ID: 18813132)
1. 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]
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. 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]
4. 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]
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. Population screening for fragile-X syndrome.
Bonthron D; Strain L
Lancet; 1993 Mar; 341(8847):769-70. PubMed ID: 8095681
[No Abstract] [Full Text] [Related]
7. Diagnosis and prevention of fragile-X syndrome. From the family study to the population screening programme: eighteen years of activity.
Giovannucci Uzielli ML; Guarducci S; Cecconi A; Lenzi S; Ricci U; Balestrieri C; Petrocelli P; Lapi E
Acta Genet Med Gemellol (Roma); 1996; 45(1-2):303-8. PubMed ID: 8872054
[No Abstract] [Full Text] [Related]
8. Molecular genetic screening in cytogenetically normal mentally retarded males with manifestations of fragile X syndrome.
Butler MG; Pratesi R; Vnencak-Jones CL
Am J Med Genet; 1994 Jul; 51(4):315-6. PubMed ID: 7942993
[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. You can build it ... but will they come?: the potential "expansion" of testing methodologies for fragile X syndrome.
Potter NT
J Mol Diagn; 2009 Jul; 11(4):279-80. PubMed ID: 19460939
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Diagnosis and screening of fragile X syndrome: experiences in Taiwan.
Lin SJ
Acta Paediatr Taiwan; 2004; 45(2):67-8. PubMed ID: 15335112
[No Abstract] [Full Text] [Related]
14. Expanded carrier screening and the law of unintended consequences: from cystic fibrosis to fragile X.
Grody WW
Genet Med; 2011 Dec; 13(12):996-7. PubMed ID: 22134443
[No Abstract] [Full Text] [Related]
15. The fragile-X syndrome: a growing gene causing familial intellectual disability.
De Vries LB; Halley DJ; Oostra BA; Niermeijer MF
J Intellect Disabil Res; 1994 Feb; 38 ( Pt 1)():1-8. PubMed ID: 8173220
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. "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]
18. Fragile X syndrome testing in the North West.
Smith K; Chandler K; Hindley D; Ramsden SC
Arch Dis Child; 2013 Mar; 98(3):239. PubMed ID: 23334255
[No 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. Ask the expert. Genetic testing for fragile X.
Prows CA; Lovell AM
J Soc Pediatr Nurs; 1998; 3(4):161-6. PubMed ID: 9884950
[No Abstract] [Full Text] [Related]
[Next] [New Search]