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Page 1
The fragile X syndrome.
Hoogeveen AT, Oostra BA. Hoogeveen AT, et al. Among authors: oostra ba. J Inherit Metab Dis. 1997 Jun;20(2):139-51. doi: 10.1023/a:1005392319533. J Inherit Metab Dis. 1997. PMID: 9211186 Review.
Normal phenotype in two brothers with a full FMR1 mutation.
Smeets HJ, Smits AP, Verheij CE, Theelen JP, Willemsen R, van de Burgt I, Hoogeveen AT, Oosterwijk JC, Oostra BA. Smeets HJ, et al. Among authors: oostra ba. Hum Mol Genet. 1995 Nov;4(11):2103-8. doi: 10.1093/hmg/4.11.2103. Hum Mol Genet. 1995. PMID: 8589687
Animal model for fragile X syndrome.
Oostra BA, Hoogeveen AT. Oostra BA, et al. Ann Med. 1997 Dec;29(6):563-7. doi: 10.3109/07853899709007483. Ann Med. 1997. PMID: 9562525 Free article. Review.
Characterization of FMR1 proteins isolated from different tissues.
Verheij C, de Graaff E, Bakker CE, Willemsen R, Willems PJ, Meijer N, Galjaard H, Reuser AJ, Oostra BA, Hoogeveen AT. Verheij C, et al. Among authors: oostra ba. Hum Mol Genet. 1995 May;4(5):895-901. doi: 10.1093/hmg/4.5.895. Hum Mol Genet. 1995. PMID: 7633450
FMRP is associated to the ribosomes via RNA.
Tamanini F, Meijer N, Verheij C, Willems PJ, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: oostra ba. Hum Mol Genet. 1996 Jun;5(6):809-13. doi: 10.1093/hmg/5.6.809. Hum Mol Genet. 1996. PMID: 8776596
560 results