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.
110 related articles for article (PubMed ID: 9494916)
1. Screening for fragile X. Berry AC J Med Screen; 1997; 4(4):247. PubMed ID: 9494916 [No Abstract] [Full Text] [Related]
2. Current controversies in prenatal diagnosis 1: screening for fragile X syndrome. Yaron Y; Musci T; Cuckle H Prenat Diagn; 2013 Jan; 33(1):6-8. PubMed ID: 23079963 [No Abstract] [Full Text] [Related]
3. Fragile X screening: what is the real issue? Laxova R Am J Med Genet; 1995 Jul; 57(3):508-9. PubMed ID: 7677165 [No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. 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; 51(4):463-5. PubMed ID: 7943020 [TBL] [Abstract][Full Text] [Related]
7. Prenatal genetic counseling: what is fragile X? Bodurtha J; Tams L; Jackson-Cook C Va Med Q; 1992; 119(2):97-8. PubMed ID: 1562624 [No Abstract] [Full Text] [Related]
8. Fragile X screening: what is the real issue? Howard-Peebles PN; Maddalena A; Spence WC; Levinson G; Fallon L; Bick DP; Black SH; Schulman JD Am J Med Genet; 1994 Dec; 53(4):382. PubMed ID: 7864051 [No Abstract] [Full Text] [Related]
10. Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test. Brown WT; Houck GE; Jeziorowska A; Levinson FN; Ding X; Dobkin C; Zhong N; Henderson J; Brooks SS; Jenkins EC JAMA; 1993 Oct; 270(13):1569-75. PubMed ID: 8371467 [TBL] [Abstract][Full Text] [Related]
11. Fragile X syndrome: diagnostic and carrier testing. Working Group of the Genetic Screening Subcommittee of the Clinical Practice Committee. American College of Medical Genetics. Am J Med Genet; 1994 Dec; 53(4):380-1. PubMed ID: 7864050 [No Abstract] [Full Text] [Related]
12. Economic evaluation of prenatal carrier screening for fragile X syndrome. Vintzileos AM; Ananth CV; Fisher AJ; Smulian JC; Day-Salvatore D; Beazoglou T; Knuppel RA J Matern Fetal Med; 1999; 8(4):168-72. PubMed ID: 10406300 [TBL] [Abstract][Full Text] [Related]
13. Who should be tested for fragile X carriership? A review of 1 center's pedigrees. Rajendra K; Bringman JJ; Ward J; Phillips OP Am J Obstet Gynecol; 2008 May; 198(5):e51-3. PubMed ID: 18358452 [TBL] [Abstract][Full Text] [Related]
14. The usefulness of cytogenetic and DNA linkage analysis in counseling families with fragile X syndrome. Silverman AC; Thibodeau SN; Jirikowic J; Hagerman RJ Birth Defects Orig Artic Ser; 1990; 26(3):238-53. PubMed ID: 2092851 [No Abstract] [Full Text] [Related]
15. [Problems posed by genetic diseases, concerning DNA instability disorders: fragile X syndrome]. Lesca G; Rousselle C Rev Prat; 2006 Oct; 56(15):1705-10. PubMed ID: 17137259 [No Abstract] [Full Text] [Related]
16. Fragile X syndrome. de la Cruz FF Am J Ment Defic; 1985 Sep; 90(2):119-23. PubMed ID: 3901755 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis and carrier screening for fragile X by PCR. Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Stark-Houck S; Brophy P; Duncan C; Dobkin C; Jenkins E Am J Med Genet; 1996 Jul; 64(1):191-5. PubMed ID: 8826474 [TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. Fragile X transmission and the determination of carrier probabilities for genetic counseling. Mulley JC; Sutherland GR Am J Med Genet; 1987 Apr; 26(4):987-90. PubMed ID: 3591842 [No Abstract] [Full Text] [Related] [Next] [New Search]