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.
192 related articles for article (PubMed ID: 15965543)
1. Fragile X syndrome: an update and review for the primary pediatrician. Visootsak J; Warren ST; Anido A; Graham JM Clin Pediatr (Phila); 2005 Jun; 44(5):371-81. PubMed ID: 15965543 [TBL] [Abstract][Full Text] [Related]
2. Health supervision for children with fragile X syndrome. Hersh JH; Saul RA; Pediatrics; 2011 May; 127(5):994-1006. PubMed ID: 21518720 [TBL] [Abstract][Full Text] [Related]
3. No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey. Bailey DB; Raspa M; Bishop E; Holiday D Pediatrics; 2009 Aug; 124(2):527-33. PubMed ID: 19581269 [TBL] [Abstract][Full Text] [Related]
4. Diagnosis and management of fragile X syndrome. Wattendorf DJ; Muenke M Am Fam Physician; 2005 Jul; 72(1):111-3. PubMed ID: 16035691 [TBL] [Abstract][Full Text] [Related]
5. Fragile-X mental retardation syndrome transmitted through intellectually normal males: implications for genetic counseling. Young RS; Jaramillo C; McCombs JL; Moore CM; Jorgenson RJ South Med J; 1986 Apr; 79(4):405-9. PubMed ID: 3704696 [TBL] [Abstract][Full Text] [Related]
6. Clinical consult: developmental delay/fragile X syndrome. Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS Prim Care; 2004 Sep; 31(3):621-5, x. PubMed ID: 15331251 [TBL] [Abstract][Full Text] [Related]
7. Molecular screening for fragile X syndrome in Thailand. Limprasert P; Ruangdaraganon N; Sura T; Vasiknanonte P; Jinorose U Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():114-8. PubMed ID: 11400746 [TBL] [Abstract][Full Text] [Related]
8. [Retrospective study of nine Lebanese families with fragile X syndrome and review of the literature]. Zafatayeff S; Zahed L; Souraty N; Megarbane A J Med Liban; 1998; 46(6):317-20. PubMed ID: 10349270 [TBL] [Abstract][Full Text] [Related]
9. [Tremor/ataxia syndrome related to Fragile X premutation]. Sallansonnet-Froment M; De Greslan T; Roux X; Bounolleau P; Ouologuem M; Taillia H; Ricard D; Renard JL Presse Med; 2010 Feb; 39(2):187-95. PubMed ID: 19419833 [TBL] [Abstract][Full Text] [Related]
10. Autism in association with fragile X syndrome in females: implications for diagnosis and treatment in children. Edwards DR; Keppen LD; Ranells JD; Gollin SM Neurotoxicology; 1988; 9(3):359-65. PubMed ID: 3200505 [TBL] [Abstract][Full Text] [Related]
11. Fragile X syndrome. Welch JL; Williams JK Neonatal Netw; 1999 Sep; 18(6):15-22. PubMed ID: 10690095 [TBL] [Abstract][Full Text] [Related]
12. Genetic analysis of fragile X-syndrome. Badaruddoza ; Shadab GG; Afzal M; Ahmad MD Indian J Med Sci; 2000 May; 54(5):174-6. PubMed ID: 11216325 [TBL] [Abstract][Full Text] [Related]
13. [Molecular diagnosis of fragile X syndrome]. Ben Jemaa L; Khemir S; Maazoul F; Richard L; Beldjord C; Chaabouni M; Chaabouni H Tunis Med; 2008 Nov; 86(11):973-7. PubMed ID: 19213487 [TBL] [Abstract][Full Text] [Related]
14. Fragile X syndrome. Wiebe E; Wiebe A Can Fam Physician; 1994 Feb; 40():290-5. PubMed ID: 8130676 [TBL] [Abstract][Full Text] [Related]
15. Checklist assessments of FMR1 gene mutation phenotypes. Johnson VA J Cult Divers; 2008; 15(3):117-31. PubMed ID: 19025200 [TBL] [Abstract][Full Text] [Related]
16. [Hair root fragile X mental retardation protein assay for the diagnosis of fragile X syndrome]. Luo XF; Zhong JM; Zhang XZ; Zou Y; Chen Y; Wu HP; Yu XY Zhongguo Dang Dai Er Ke Za Zhi; 2009 Oct; 11(10):817-20. PubMed ID: 19849940 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Molecular diagnosis and genetic counseling for fragile X mental retardation. Pandey UB; Phadke SR; Mittal B Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237 [TBL] [Abstract][Full Text] [Related]
19. A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause. Limprasert P; Ruangdaraganon N; Vasiknanonte P; Sura T; Jaruratanasirikul S; Sriwongpanich N; Sriplung H J Med Assoc Thai; 2000 Oct; 83(10):1260-6. PubMed ID: 11143494 [TBL] [Abstract][Full Text] [Related]