Verkerk AJ - Search Results

1

A point mutation in the FMR-1 gene associated with fragile X mental retardation.

De Boulle K, Verkerk AJ, Reyniers E, Vits L, Hendrickx J, Van Roy B, Van den Bos F, de Graaff E, Oostra BA, Willems PJ. De Boulle K, et al. Among authors: verkerk aj. Nat Genet. 1993 Jan;3(1):31-5. doi: 10.1038/ng0193-31. Nat Genet. 1993. PMID: 8490650

2

The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation.

Oostra BA, Verkerk AJ. Oostra BA, et al. Among authors: verkerk aj. Chromosoma. 1992 Apr;101(7):381-7. doi: 10.1007/BF00582832. Chromosoma. 1992. PMID: 1618021 Review.

3

Mental status and fragile X expression in relation to FMR-1 gene mutation.

de Vries BB, Wiegers AM, de Graaff E, Verkerk AJ, Van Hemel JO, Halley DJ, Fryns JP, Curfs LM, Niermeijer MF, Oostra BA. de Vries BB, et al. Among authors: verkerk aj. Eur J Hum Genet. 1993;1(1):72-9. doi: 10.1159/000472389. Eur J Hum Genet. 1993. PMID: 8069653

4

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

Reyniers E, Vits L, De Boulle K, Van Roy B, Van Velzen D, de Graaff E, Verkerk AJ, Jorens HZ, Darby JK, Oostra B, et al. Reyniers E, et al. Among authors: verkerk aj. Nat Genet. 1993 Jun;4(2):143-6. doi: 10.1038/ng0693-143. Nat Genet. 1993. PMID: 8348152

5

Alternative splicing in the fragile X gene FMR1.

Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al. Verkerk AJ, et al. Hum Mol Genet. 1993 Apr;2(4):399-404. doi: 10.1093/hmg/2.4.399. Hum Mol Genet. 1993. PMID: 8504300

6

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: verkerk aj. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

7

Segregation of the fragile X mutation from an affected male to his normal daughter.

Willems PJ, Van Roy B, De Boulle K, Vits L, Reyniers E, Beck O, Dumon JE, Verkerk A, Oostra B. Willems PJ, et al. Hum Mol Genet. 1992 Oct;1(7):511-5. doi: 10.1093/hmg/1.7.511. Hum Mol Genet. 1992. PMID: 1307252

8

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. 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

9

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. 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

10

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL. Parrish JE, et al. Among authors: verkerk aj. Nat Genet. 1994 Nov;8(3):229-35. doi: 10.1038/ng1194-229. Nat Genet. 1994. PMID: 7874164

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