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.
83 related articles for article (PubMed ID: 7943019)
1. Counselling risk figures for fragile X carrier females of varying band sizes for use in predicting the likelihood of retardation in their offspring. Turner AM; Robinson H; Wake S; Laing SJ; Leigh D; Turner G Am J Med Genet; 1994 Jul; 51(4):458-62. PubMed ID: 7943019 [TBL] [Abstract][Full Text] [Related]
2. Fragile X syndrome. Laxova R Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687 [TBL] [Abstract][Full Text] [Related]
3. Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses. Sherman SL; Maddalena A; Howard-Peebles PN; Brown WT; Nolin S; Jenkins E; Schwartz C; Tarrelton J; Shapiro LR; Smits AP Am J Med Genet; 1994 Jul; 51(4):503-6. PubMed ID: 7943029 [TBL] [Abstract][Full Text] [Related]
4. [A genetic and molecular study of 85 families affected with the fragile X syndrome]. Milà Recasens M; Sánchez Díaz A; Glover López G; Castellví Bel S; Carbonell Meseguer P; Kruyer H; Ballesta Martínez F; Estivill Pallejà X An Esp Pediatr; 1996 Mar; 44(3):250-6. PubMed ID: 8830601 [TBL] [Abstract][Full Text] [Related]
5. Screening for fragile X syndrome. Murray J; Cuckle H; Taylor G; Hewison J Health Technol Assess; 1997; 1(4):i-iv, 1-71. PubMed ID: 9414543 [TBL] [Abstract][Full Text] [Related]
6. Molecular-neurobehavioral associations in females with the fragile X full mutation. Abrams MT; Reiss AL; Freund LS; Baumgardner TL; Chase GA; Denckla MB Am J Med Genet; 1994 Jul; 51(4):317-27. PubMed ID: 7942994 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues. Mandel JL; Biancalana V Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801 [TBL] [Abstract][Full Text] [Related]
10. Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome. Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJ; Horst J; Mazurczak T Acta Biochim Pol; 1996; 43(2):383-8. PubMed ID: 8862184 [TBL] [Abstract][Full Text] [Related]
11. [A clinical and molecular genetic analysis of the fragile X syndrome]. Bychkova AM; Maliarchuk SG; Livshits LA Tsitol Genet; 1999; 33(4):70-6. PubMed ID: 10563381 [TBL] [Abstract][Full Text] [Related]
12. Dilemmas in counselling females with the fragile X syndrome. de Vries BB; van den Boer-van den Berg HM; Niermeijer MF; Tibben A J Med Genet; 1999 Feb; 36(2):167-70. PubMed ID: 10051021 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Recurrence risks for relatives in families with an isolated case of the fragile X syndrome. Sherman SL; Rogatko A; Turner G Am J Med Genet; 1988 Dec; 31(4):753-65. PubMed ID: 3239564 [TBL] [Abstract][Full Text] [Related]
15. Reverse mutations in the fragile X syndrome. Brown WT; Houck GE; Ding X; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Am J Med Genet; 1996 Aug; 64(2):287-92. PubMed ID: 8844067 [TBL] [Abstract][Full Text] [Related]
16. Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase. Chong SS; Eichler EE; Nelson DL; Hughes MR Am J Med Genet; 1994 Jul; 51(4):522-6. PubMed ID: 7943034 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing. Hagerman RJ; Wilson P; Staley LW; Lang KA; Fan T; Uhlhorn C; Jewell-Smart S; Hull C; Drisko J; Flom K Am J Med Genet; 1994 Jul; 51(4):474-81. PubMed ID: 7943023 [TBL] [Abstract][Full Text] [Related]
18. Prediction of mental status in carriers of the fragile X mutation using CGG repeat length. Smits A; Smeets D; Hamel B; Dreesen J; de Haan A; van Oost B Am J Med Genet; 1994 Jul; 51(4):497-500. PubMed ID: 7943027 [TBL] [Abstract][Full Text] [Related]
19. [DNA diagnosis of fragile X syndrome in a family. A new type of heredity--dynamic mutations]. Eiken HG; Boman H; Apold J Tidsskr Nor Laegeforen; 1993 Oct; 113(26):3236-9. PubMed ID: 8236216 [TBL] [Abstract][Full Text] [Related]
20. DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene. van den Ouweland AM; de Vries BB; Bakker PL; Deelen WH; de Graaff E; van Hemel JO; Oostra BA; Niermeijer MF; Halley DJ Am J Med Genet; 1994 Jul; 51(4):482-5. PubMed ID: 7943024 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]