van Oost BA - Search Results

1

Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.

Oostra BA, Majoor-Krakauer DF, van Hemel JO, Bakker E, Callen DF, Schmidt M, van Oost BA. Oostra BA, et al. Among authors: van oost ba, van hemel jo. Am J Med Genet. 1991 Feb-Mar;38(2-3):332-5. doi: 10.1002/ajmg.1320380233. Am J Med Genet. 1991. PMID: 1673306

2

Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe.

van Oost BA, Smits AP, Dreesen JC, van den Ouweland AM, Oostra BA. van Oost BA, et al. Among authors: van den ouweland am. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):320-7. doi: 10.1002/ajmg.1320430149. Am J Med Genet. 1992. PMID: 1605205

3

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: van oost ba. Hum Genet. 1991 Jul;87(3):369-72. doi: 10.1007/BF00200922. Hum Genet. 1991. PMID: 1677926 Free article.

4

RN1, a new polymorphic marker near the fragile X locus. (HGM10 assignment DXS 369).

Hupkes PE, van Bennekom CA, van Oost BA, Oostra BA. Hupkes PE, et al. Among authors: van oost ba, van bennekom ca. Nucleic Acids Res. 1990 Feb 11;18(3):692. doi: 10.1093/nar/18.3.692-a. Nucleic Acids Res. 1990. PMID: 1968631 Free PMC article.

5

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: van bennekom ca. Am J Med Genet. 1991 Feb-Mar;38(2-3):328-31. doi: 10.1002/ajmg.1320380232. Am J Med Genet. 1991. PMID: 2018075

6

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: van oost 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.

7

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site.

Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, van Oost BA, Smits AP, Ramos FJ, Pfendner E, et al. Riggins GJ, et al. Among authors: van oost ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):237-43. doi: 10.1002/ajmg.1320430138. Am J Med Genet. 1992. PMID: 1605197

8

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: van oost ba. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

9

Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.

Smits A, Smeets D, Hamel B, Dreesen J, de Haan A, van Oost B. Smits A, et al. Am J Med Genet. 1994 Jul 15;51(4):497-500. doi: 10.1002/ajmg.1320510440. Am J Med Genet. 1994. PMID: 7943027

10

Prenatal exclusion of choroideremia.

van den Hurk JA, van Zandvoort PM, Brunsmann F, Pawlowitzki IH, Holzgreve W, Szabo P, Cremers FP, van Oost BA. van den Hurk JA, et al. Among authors: van oost ba, van zandvoort pm. Am J Med Genet. 1992 Dec 1;44(6):822-3. doi: 10.1002/ajmg.1320440621. Am J Med Genet. 1992. PMID: 1362326

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