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Severe mental retardation and macroorchidism without mutation in the FMR1 gene.
Reyniers E, Wolff G, Tariverdian G, De Boulle K, Storm K, Kooy RF, Willems PJ. Reyniers E, et al. Among authors: de boulle k. Am J Med Genet. 1996 Aug 9;64(2):408-12. doi: 10.1002/(SICI)1096-8628(19960809)64:2<408::AID-AJMG35>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8844093 Review.
Alternative splicing in the fragile X gene FMR1.
Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al. Verkerk AJ, et al. Among authors: de graaff e, de boulle k. Hum Mol Genet. 1993 Apr;2(4):399-404. doi: 10.1093/hmg/2.4.399. Hum Mol Genet. 1993. PMID: 8504300
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: de deyn pp, de boulle k. 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
Long-term potentiation in the hippocampus of fragile X knockout mice.
Godfraind JM, Reyniers E, De Boulle K, D'Hooge R, De Deyn PP, Bakker CE, Oostra BA, Kooy RF, Willems PJ. Godfraind JM, et al. Among authors: de deyn pp, de boulle k. Am J Med Genet. 1996 Aug 9;64(2):246-51. doi: 10.1002/(SICI)1096-8628(19960809)64:2<246::AID-AJMG2>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8844057
An EcoRI RFLP in the 5' region of the human NF1 gene.
Reyniers E, De Boulle K, Marchuk DA, Andersen LB, Collins FS, Willems PJ. Reyniers E, et al. Among authors: de boulle k. Hum Genet. 1993 Dec;92(6):631. doi: 10.1007/BF00420953. Hum Genet. 1993. PMID: 7903272 Free article.
75 results