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.
375 related articles for article (PubMed ID: 6237176)
41. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features. Wiegers AM; Curfs LM; Meijer H; Oostra B; Fryns JP Genet Couns; 1994; 5(4):377-80. PubMed ID: 7888141 [TBL] [Abstract][Full Text] [Related]
42. [Fragile X chromosome and X-linked mental retardation (author's transl)]. Fonatsch C; Flatz SD Wien Klin Wochenschr; 1982 Apr; 94(8):217-9. PubMed ID: 7101956 [TBL] [Abstract][Full Text] [Related]
43. Implications of fragile X expression in normal males for the nature of the mutation. Ledbetter DH; Ledbetter SA; Nussbaum RL Nature; 1986 Nov 13-19; 324(6093):161-3. PubMed ID: 3785381 [TBL] [Abstract][Full Text] [Related]
44. [Fragile X syndrome. Diagnosis, genetics and clinical findings]. Hjalgrim H; Grønskov K; Brøndum-Nielsen K Ugeskr Laeger; 1998 Sep; 160(37):5330-4. PubMed ID: 9748856 [TBL] [Abstract][Full Text] [Related]
45. Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin. Carpenter NJ; Leichtman LG; Say B Am J Dis Child; 1982 May; 136(5):392-8. PubMed ID: 7081157 [TBL] [Abstract][Full Text] [Related]
46. [Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families]. Rodríguez Costa T; Gabarrón Llamas J; Casas Fernández C; Glover López G; Puche Mira A; Jiménez Cocina A An Esp Pediatr; 1984 Oct; 21 Suppl 20():54-7. PubMed ID: 6595955 [No Abstract] [Full Text] [Related]
47. Brief report: linkage between G6PD and fragile-X syndrome. Filippi G; Rinaldi A; Archidiacono N; Rocchi M; Balazs I; Siniscalco M Am J Med Genet; 1983 May; 15(1):113-9. PubMed ID: 6602550 [TBL] [Abstract][Full Text] [Related]
48. [X-linked mental retardation and X-chromosome fragile sites (author's transl)]. Schmidt A; Passarge E Dtsch Med Wochenschr; 1981 Apr; 106(15):460-3. PubMed ID: 7215173 [TBL] [Abstract][Full Text] [Related]
49. Fragile X-linked mental retardation, a new entity: case reports. Kelly TE; Shires MA; Harris L; Wyandt H; Wilson WG Va Med; 1983 Apr; 110(4):250-2. PubMed ID: 6868782 [No Abstract] [Full Text] [Related]
50. X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families). Archidiacono N; Rocchi M; Rinaldi A; Filippi G J Genet Hum; 1987 Dec; 35(5):381-98. PubMed ID: 3437266 [TBL] [Abstract][Full Text] [Related]
51. [Fragile X chromosome syndrome: a chromosomal defect associated with mental retardation]. Santos M; Morizon G Rev Med Chil; 1983 Jun; 111(6):597-600. PubMed ID: 6669807 [No Abstract] [Full Text] [Related]
52. Fragile X syndrome. Laxova R Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687 [TBL] [Abstract][Full Text] [Related]
53. [Mental retardation and the fragile X syndrome]. Veenema H; Geraedts JP Ned Tijdschr Geneeskd; 1984 Mar; 128(13):618-21. PubMed ID: 6717630 [No Abstract] [Full Text] [Related]
54. [[Incidence of X-chromosome fragility in medium and severe mental retardation]. Szakmáry E; Tomsits E; Vass M; Schuler D Orv Hetil; 1984 May; 125(20):1195-9. PubMed ID: 6718007 [No Abstract] [Full Text] [Related]
55. [The clinico-genetic aspects of mental retardation related to the fragile-X chromosome]. Viekhova NV; Demydova IA; Bychkova HM; Vorsanova SH; Buzhiievs'ka TI Tsitol Genet; 1992; 26(6):64-71. PubMed ID: 1292164 [TBL] [Abstract][Full Text] [Related]
56. 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]
57. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families. Schinzel A; Largo RH Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245 [TBL] [Abstract][Full Text] [Related]
58. Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome). Jennings M; Hall JG; Hoehn H Am J Med Genet; 1980; 7(4):417-32. PubMed ID: 6938131 [TBL] [Abstract][Full Text] [Related]