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221 related items for PubMed ID: 8826442
1. Seventh International Workshop on the Fragile X and X-linked Mental Retardation. Tranebjaerg L, Lubs HA, Borghgraef M, Brown WT, Fisch G, Fryns JP, Hagerman R, Jacobs PA, Mandel JL, Mulley J, Oostra B, Schwartz C, Sherman S, Willard H, Willems P. Am J Med Genet; 1996 Jul 12; 64(1):1-14. PubMed ID: 8826442 [No Abstract] [Full Text] [Related]
2. 9th international workshop on fragile X syndrome and X-linked mental retardation. Fryns JP, Borghgraef M, Brown TW, Chelly J, Fisch GS, Hamel B, Hanauer A, Lacombe D, Luo L, MacPherson JN, Mandel JL, Moraine C, Mulley J, Nelson D, Oostra B, Partington M, Ramakers GJ, Ropers HH, Rousseau F, Schwartz C, Steinbach P, Stoll C, Tranebjaerg L, Turner G, Van Bokhoven H, Vianna-Morgante A. Am J Med Genet; 2000 Oct 23; 94(5):345-60. PubMed ID: 11050616 [No Abstract] [Full Text] [Related]
3. X-linked mental retardation: caveats in genetic counselling. Partington MW. Am J Med Genet; 1986 Oct 23; 23(1-2):101-9. PubMed ID: 3953640 [No Abstract] [Full Text] [Related]
4. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. Brown WT, Jenkins E, Neri G, Lubs H, Shapiro LR, Davies KE, Sherman S, Hagerman R, Laird C. Am J Med Genet; 1991 Oct 23; 38(2-3):158-72. PubMed ID: 1673296 [No Abstract] [Full Text] [Related]
5. X-linked mental retardation. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. Am J Med Genet; 1991 Oct 23; 38(2-3):153. PubMed ID: 1673295 [No Abstract] [Full Text] [Related]
6. Fragile X syndrome: a major cause of X-linked mental retardation. Butler MG. Compr Ther; 1988 Jul 23; 14(7):3-7. PubMed ID: 3060303 [No Abstract] [Full Text] [Related]
7. 6th International Workshop on the Fragile X and X-Linked Mental Retardation. Cairns, Northern Australia, 3-6 August 1993. Proceedings and abstracts. Am J Med Genet; 1994 Jul 15; 51(4):281-618. PubMed ID: 7942988 [No Abstract] [Full Text] [Related]
8. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe. Choo KH, George D, Filby G, Halliday JL, Leversha M, Webb G, Danks DM. Lancet; 1984 Aug 11; 2(8398):349. PubMed ID: 6146889 [No Abstract] [Full Text] [Related]
9. Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988). Spano LM, Opitz JM. Am J Med Genet; 1988 Aug 11; 30(1-2):31-60. PubMed ID: 3052063 [No Abstract] [Full Text] [Related]
10. The strength of association between fragile (X) chromosome presence and mental retardation. Silverman W, Lubin R, Jenkins EC, Brown WT. Clin Genet; 1983 Jun 11; 23(6):436-40. PubMed ID: 6684008 [Abstract] [Full Text] [Related]
11. DNA studies of X-linked mental retardation associated with a fragile site at Xq27. Davies KE. Am J Med Genet; 1986 Jun 11; 23(1-2):633-42. PubMed ID: 3513572 [Abstract] [Full Text] [Related]
12. The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects. Gecz J. Ann Hum Genet; 2000 Mar 11; 64(Pt 2):95-106. PubMed ID: 11246464 [Abstract] [Full Text] [Related]
13. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome. Bell MV, Hirst MC, Nakahori Y, MacKinnon RN, Roche A, Flint TJ, Jacobs PA, Tommerup N, Tranebjaerg L, Froster-Iskenius U. Cell; 1991 Feb 22; 64(4):861-6. PubMed ID: 1997211 [Abstract] [Full Text] [Related]
14. Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians. Zhong N, Ju W, Xu W, Ye L, Shen Y, Wu G, Chen SH, Jin R, Hu XF, Yang A, Liu X, Poon P, Pang C, Zheng Y, Song L, Zhao P, Fu B, Gu H, Brown WT. Am J Med Genet; 1999 May 28; 84(3):191-4. PubMed ID: 10331588 [Abstract] [Full Text] [Related]
15. Non-specific X-linked mental retardation: background, types, diagnosis and prevalence. Howard-Peebles PN. J Ment Defic Res; 1982 Dec 28; 26 (Pt 4)():205-13. PubMed ID: 6763078 [Abstract] [Full Text] [Related]
16. Some problems in the genetics of X-linked mental retardation. Tariverdian G, Vogel F. Cytogenet Cell Genet; 2000 Dec 28; 91(1-4):278-84. PubMed ID: 11173869 [Abstract] [Full Text] [Related]
17. Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation. Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Hum Genet; 2000 Jan 28; 106(1):36-9. PubMed ID: 10982179 [Abstract] [Full Text] [Related]
18. Fifth international workshop on fragile X and X-linked mental retardation. Mandel JL, Hagerman R, Froster U, Brown WT, Jenkins EC, Jacobs P, TurnerG, Lubs H, Neri G. Am J Med Genet; 2000 Jan 28; 43(1-2):5-27. PubMed ID: 1605233 [No Abstract] [Full Text] [Related]
19. Recurrence risks in mental retardation. Crow YJ, Tolmie JL. J Med Genet; 1998 Mar 28; 35(3):177-82. PubMed ID: 9541099 [Abstract] [Full Text] [Related]
20. [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 28; 86(11):973-7. PubMed ID: 19213487 [Abstract] [Full Text] [Related] Page: [Next] [New Search]