Oostra 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. 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

Limited size of the fragile X site shown by fluorescence in situ hybridization.

Verkerk AJ, Eussen BH, Van Hemel JO, Oostra BA. Verkerk AJ, et al. Among authors: oostra ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):187-91. doi: 10.1002/ajmg.1320430131. Am J Med Genet. 1992. PMID: 1605191

3

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: oostra ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

4

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: oostra ba. 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

5

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.

6

DNA analysis in patients with lissencephaly type I and other cortical dysplasias.

Oostra BA, de Rijk-van Andel JF, Eussen HJ, van Hemel JO, Halley DJ, Niermeijer MF. Oostra BA, et al. Am J Med Genet. 1991 Sep 1;40(3):383-6. doi: 10.1002/ajmg.1320400328. Am J Med Genet. 1991. PMID: 1951447

7

New polymorphic DNA marker close to the fragile site FRAXA.

Oostra BA, Hupkes PE, Perdon LF, van Bennekom CA, Bakker E, Halley DJ, Schmidt M, Du Sart D, Smits A, Wieringa B, et al. Oostra BA, et al. Genomics. 1990 Jan;6(1):129-32. doi: 10.1016/0888-7543(90)90457-6. Genomics. 1990. PMID: 1968042 Free article.

8

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: oostra ba. 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.

9

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

10

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.

van den Ouweland AM, de Vries BB, Bakker PL, Deelen WH, de Graaff E, van Hemel JO, Oostra BA, Niermeijer MF, Halley DJ. van den Ouweland AM, et al. Among authors: oostra ba. Am J Med Genet. 1994 Jul 15;51(4):482-5. doi: 10.1002/ajmg.1320510437. Am J Med Genet. 1994. PMID: 7943024

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