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New distal marker closely linked to the fragile X locus.
Hulsebos TJ, Oostra BA, Broersen S, Smits A, van Oost BA, Westerveld A. Hulsebos TJ, et al. Among authors: oostra ba. Hum Genet. 1991 Jul;87(3):369-72. doi: 10.1007/BF00200922. Hum Genet. 1991. PMID: 1677926 Free article.
Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.
van Oost BA, Smits A, Dreesen JC, Smeets D, Perdon L, van Bennekom CA, Dahl N, Bakker E, Oostra BA. van Oost BA, et al. Among authors: oostra ba. Am J Med Genet. 1991 Feb-Mar;38(2-3):328-31. doi: 10.1002/ajmg.1320380232. Am J Med Genet. 1991. PMID: 2018075
The fragile X syndrome: no evidence for any recent mutations.
Smits AP, Dreesen JC, Post JG, Smeets DF, de Die-Smulders C, Spaans-van der Bijl T, Govaerts LC, Warren ST, Oostra BA, van Oost BA. Smits AP, et al. Among authors: oostra ba. J Med Genet. 1993 Feb;30(2):94-6. doi: 10.1136/jmg.30.2.94. J Med Genet. 1993. PMID: 8445628 Free PMC article.
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
Mental status of females with an FMR1 gene full mutation.
de Vries BB, Wiegers AM, Smits AP, Mohkamsing S, Duivenvoorden HJ, Fryns JP, Curfs LM, Halley DJ, Oostra BA, van den Ouweland AM, Niermeijer MF. de Vries BB, et al. Among authors: oostra ba. Am J Hum Genet. 1996 May;58(5):1025-32. Am J Hum Genet. 1996. PMID: 8651263 Free PMC article.
560 results