112 related articles for article (PubMed ID: 9393231)
1. Case finding for the fragile X syndrome and its consequences.
Turner G; Robinson H; Wake S; Laing S; Partington M
BMJ; 1997 Nov; 315(7117):1223-6. PubMed ID: 9393231
[No Abstract] [Full Text] [Related]
2. Population screening for fragile X.
Turner G; Robinson H; Laing S; van den Berk M; Colley A; Goddard A; Sherman S; Partington M
Lancet; 1992 May; 339(8803):1210-3. PubMed ID: 1349946
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Should all pregnant women be offered carrier testing for fragile X syndrome?
Finucane B
Clin Obstet Gynecol; 1996 Dec; 39(4):772-82. PubMed ID: 8934029
[No Abstract] [Full Text] [Related]
5. Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general.
Fryns JP
Genet Couns; 1995; 6(4):293-6. PubMed ID: 8775414
[No Abstract] [Full Text] [Related]
6. Population based prenatal screening for the fragile X syndrome.
Palomaki GE
J Med Screen; 1994 Jan; 1(1):65-72. PubMed ID: 8790488
[No Abstract] [Full Text] [Related]
7. [Screening for carriers of the fragile X syndrome; ethical exploration].
de Jong A; de Wert G
Ned Tijdschr Geneeskd; 2002 Mar; 146(13):611-5. PubMed ID: 11957380
[TBL] [Abstract][Full Text] [Related]
8. Informed choice in fragile X syndrome and its effects on prevalence.
Robinson H; Wake S; Wright F; Laing S; Turner G
Am J Med Genet; 1996 Jul; 64(1):198-202. PubMed ID: 8826476
[TBL] [Abstract][Full Text] [Related]
9. [Genetics of Fragile X syndrome and its prevention].
Boué J; Simon-Bouy B
J Gynecol Obstet Biol Reprod (Paris); 1997; 26(3):273-9. PubMed ID: 9265049
[TBL] [Abstract][Full Text] [Related]
10. Screening for fragile X syndrome: a model for genetic disorders?
Barnicoat A
BMJ; 1997 Nov; 315(7117):1174-5. PubMed ID: 9393215
[No Abstract] [Full Text] [Related]
11. Screening for fragile X syndrome: information needs for health planners.
Murray J; Cuckle H; Taylor G; Hewison J
J Med Screen; 1997; 4(2):60-94. PubMed ID: 9275266
[No Abstract] [Full Text] [Related]
12. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
[TBL] [Abstract][Full Text] [Related]
13. Clinical screening score for the fragile X (Martin-Bell) syndrome.
Laing S; Partington M; Robinson H; Turner G
Am J Med Genet; 1991; 38(2-3):256-9. PubMed ID: 2018069
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
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. Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis.
Cheng YK; Lin CS; Kwok YK; Chan YM; Lau TK; Leung TY; Choy KW
Hong Kong Med J; 2017 Apr; 23(2):110-6. PubMed ID: 28253484
[TBL] [Abstract][Full Text] [Related]
19. Is it time for population-based prenatal screening for fragile-X?
Palomaki GE; Haddow JE
Lancet; 1993 Feb; 341(8841):373-4. PubMed ID: 8094139
[No Abstract] [Full Text] [Related]
20. Characteristics of fragile X relatives with different attitudes toward terminating an affected pregnancy.
Meryash DL
Am J Ment Retard; 1992 Mar; 96(5):528-35. PubMed ID: 1562310
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]