Oostra BA - Search Results

1

Prenatal diagnosis of fragile X syndrome.

Willemsen R, Oosterwijk JC, Los FJ, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: oostra ba. Lancet. 1996 Oct 5;348(9032):967-8. doi: 10.1016/s0140-6736(05)65388-3. Lancet. 1996. PMID: 8843844 No abstract available.

2

Prenatal detection of major cystic fibrosis mutation.

Halley DJ, van Damme NH, Deelen WH, Oostra BA, Jahoda MG, Sachs ES, Los FJ, Niermeijer MF. Halley DJ, et al. Among authors: oostra ba. Lancet. 1989 Oct 21;2(8669):972. doi: 10.1016/s0140-6736(89)90973-2. Lancet. 1989. PMID: 2571875 No abstract available.

3

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA. Verheij C, et al. Among authors: oostra ba. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

4

Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique.

Willemsen R, Smits A, Mohkamsing S, van Beerendonk H, de Haan A, de Vries B, van den Ouweland A, Sistermans E, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: oostra ba. Hum Genet. 1997 Mar;99(3):308-11. doi: 10.1007/s004390050363. Hum Genet. 1997. PMID: 9050914 Free article.

5

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

Losekoot M, Hoogendoorn E, Olmer R, Jansen CC, Oosterwijk JC, van den Ouweland AM, Halley DJ, Warren ST, Willemsen R, Oostra BA, Bakker E. Losekoot M, et al. Among authors: oostra ba. J Med Genet. 1997 Nov;34(11):924-6. doi: 10.1136/jmg.34.11.924. J Med Genet. 1997. PMID: 9391887 Free PMC article.

6

Fragile X syndrome at the turn of the century.

Kooy RF, Willemsen R, Oostra BA. Kooy RF, et al. Among authors: oostra ba. Mol Med Today. 2000 May;6(5):193-8. doi: 10.1016/s1357-4310(00)01674-9. Mol Med Today. 2000. PMID: 10782066 Review.

7

FMRP detection assay for the diagnosis of the fragile X syndrome.

Willemsen R, Oostra BA. Willemsen R, et al. Among authors: oostra ba. Am J Med Genet. 2000 Fall;97(3):183-8. doi: 10.1002/1096-8628(200023)97:3<183::AID-AJMG1035>3.0.CO;2-3. Am J Med Genet. 2000. PMID: 11449486 Review.

8

The X chromosome and fragile X mental retardation.

Oostra BA, Willemsen R. Oostra BA, et al. Cytogenet Genome Res. 2002;99(1-4):257-64. doi: 10.1159/000071602. Cytogenet Genome Res. 2002. PMID: 12900573 Review.

9

In vitro reactivation of the FMR1 gene involved in fragile X syndrome.

Chiurazzi P, Pomponi MG, Willemsen R, Oostra BA, Neri G. Chiurazzi P, et al. Among authors: oostra ba. Hum Mol Genet. 1998 Jan;7(1):109-13. doi: 10.1093/hmg/7.1.109. Hum Mol Genet. 1998. PMID: 9384610

10

Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.

Tamanini F, Bontekoe C, Bakker CE, van Unen L, Anar B, Willemsen R, Yoshida M, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: oostra ba. Hum Mol Genet. 1999 May;8(5):863-9. doi: 10.1093/hmg/8.5.863. Hum Mol Genet. 1999. PMID: 10196376 Free article.

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