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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. Tranebjaerg L, et al. Among authors: willems p. Am J Med Genet. 1996 Jul 12;64(1):1-14. doi: 10.1002/(SICI)1096-8628(19960712)64:1<1::AID-AJMG1>3.0.CO;2-Z. Am J Med Genet. 1996. PMID: 8826442 No abstract available.
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.
Holden JJ, Percy M, Allingham-Hawkins D, Brown WT, Chiurazzi P, Fisch G, Gane L, Gunter C, Hagerman R, Jenkins EC, Kooy RF, Lubs HA, Murray A, Neri G, Schwartz C, Tranebjaerg L, Villard L, Willems PJ. Holden JJ, et al. Among authors: willems pj. Am J Med Genet. 1999 Apr 2;83(4):221-36. doi: 10.1002/(sici)1096-8628(19990402)83:4<221::aid-ajmg1>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10208154 No abstract available.
A fragile gene.
Oostra BA, Willems PJ. Oostra BA, et al. Among authors: willems pj. Bioessays. 1995 Nov;17(11):941-7. doi: 10.1002/bies.950171107. Bioessays. 1995. PMID: 8526888 Review.
Transgenic mouse model for the fragile X syndrome.
Kooy RF, D'Hooge R, Reyniers E, Bakker CE, Nagels G, De Boulle K, Storm K, Clincke G, De Deyn PP, Oostra BA, Willems PJ. Kooy RF, et al. Among authors: willems pj. Am J Med Genet. 1996 Aug 9;64(2):241-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<241::AID-AJMG1>3.0.CO;2-X. Am J Med Genet. 1996. PMID: 8844056
The fragile X syndrome and other fragile site disorders.
Kooy RF, Oostra BA, Willems PJ. Kooy RF, et al. Among authors: willems pj. Results Probl Cell Differ. 1998;21:1-46. doi: 10.1007/978-3-540-69680-3_1. Results Probl Cell Differ. 1998. PMID: 9670313 Review. No abstract available.
Postmortem examination of two fragile X brothers with an FMR1 full mutation.
Reyniers E, Martin JJ, Cras P, Van Marck E, Handig I, Jorens HZ, Oostra BA, Kooy RF, Willems PJ. Reyniers E, et al. Among authors: willems pj. Am J Med Genet. 1999 May 28;84(3):245-9. doi: 10.1002/(sici)1096-8628(19990528)84:3<245::aid-ajmg16>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10331601
Noninvasive test for fragile X syndrome, using hair root analysis.
Willemsen R, Anar B, De Diego Otero Y, de Vries BB, Hilhorst-Hofstee Y, Smits A, van Looveren E, Willems PJ, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: willems pj. Am J Hum Genet. 1999 Jul;65(1):98-103. doi: 10.1086/302462. Am J Hum Genet. 1999. PMID: 10364521 Free PMC article.
997 results