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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. 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.
XLMR genes: update 1996.
Lubs HA, Chiurazzi P, Arena JF, Schwartz C, Tranebjaerg L, Neri G. Lubs HA, et al. Among authors: tranebjaerg l. Am J Med Genet. 1996 Jul 12;64(1):147-57. doi: 10.1002/(SICI)1096-8628(19960712)64:1<147::AID-AJMG25>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826465 Review.
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: tranebjaerg l. 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.
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. Fryns JP, et al. Among authors: tranebjaerg l. Am J Med Genet. 2000 Oct 23;94(5):345-60. doi: 10.1002/1096-8628(20001023)94:5<345::aid-ajmg1>3.0.co;2-z. Am J Med Genet. 2000. PMID: 11050616 No abstract available.
XLMR genes: update 1998.
Lubs H, Chiurazzi P, Arena J, Schwartz C, Tranebjaerg L, Neri G. Lubs H, et al. Among authors: tranebjaerg l. Am J Med Genet. 1999 Apr 2;83(4):237-47. Am J Med Genet. 1999. PMID: 10208155 Review.
A new gene (DYX3) for dyslexia is located on chromosome 2.
Fagerheim T, Raeymaekers P, Tønnessen FE, Pedersen M, Tranebjaerg L, Lubs HA. Fagerheim T, et al. Among authors: tranebjaerg l. J Med Genet. 1999 Sep;36(9):664-9. J Med Genet. 1999. PMID: 10507721 Free PMC article.
213 results