Reyniers E - Search Results

1

CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation.

Kooy RF, Reyniers E, Storm K, Vits L, van Velzen D, de Ruiter PE, Brinkmann AO, de Paepe A, Willems PJ. Kooy RF, et al. Among authors: reyniers e. Am J Med Genet. 1999 Jul 30;85(3):209-13. Am J Med Genet. 1999. PMID: 10398229

2

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. Among authors: reyniers e. Hum Mol Genet. 1992 Oct;1(7):511-5. doi: 10.1093/hmg/1.7.511. Hum Mol Genet. 1992. PMID: 1307252

3

An EcoRI RFLP in the 5' region of the human NF1 gene.

Reyniers E, De Boulle K, Marchuk DA, Andersen LB, Collins FS, Willems PJ. Reyniers E, et al. Hum Genet. 1993 Dec;92(6):631. doi: 10.1007/BF00420953. Hum Genet. 1993. PMID: 7903272 Free article.

4

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

Vits L, Van Camp G, Coucke P, Fransen E, De Boulle K, Reyniers E, Korn B, Poustka A, Wilson G, Schrander-Stumpel C, et al. Vits L, et al. Among authors: reyniers e. Nat Genet. 1994 Jul;7(3):408-13. doi: 10.1038/ng0794-408. Nat Genet. 1994. PMID: 7920660

5

Apparent regression of the CGG repeat in FMR1 to an allele of normal size.

Vits L, De Boulle K, Reyniers E, Handig I, Darby JK, Oostra B, Willems PJ. Vits L, et al. Among authors: reyniers e. Hum Genet. 1994 Nov;94(5):523-6. doi: 10.1007/BF00211019. Hum Genet. 1994. PMID: 7959688

6

Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type I syndrome.

Beckers A, Abs R, Reyniers E, De Boulle K, Stevenaert A, Heller FR, Klöppel G, Meurisse M, Willems PJ. Beckers A, et al. Among authors: reyniers e. J Clin Endocrinol Metab. 1994 Nov;79(5):1498-502. doi: 10.1210/jcem.79.5.7962349. J Clin Endocrinol Metab. 1994. PMID: 7962349

7

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11.

Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ. Wu YQ, et al. Among authors: reyniers e. Hum Mol Genet. 1994 Jan;3(1):167-71. doi: 10.1093/hmg/3.1.167. Hum Mol Genet. 1994. PMID: 8162019

8

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. Nat Genet. 1993 Jun;4(2):143-6. doi: 10.1038/ng0693-143. Nat Genet. 1993. PMID: 8348152

9

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. Among authors: reyniers e. Hum Mol Genet. 1993 Aug;2(8):1348. doi: 10.1093/hmg/2.8.1348. Hum Mol Genet. 1993. PMID: 8401531 No abstract available.

10

Founder effect in a Belgian-Dutch fragile X population.

Buyle S, Reyniers E, Vits L, De Boulle K, Handig I, Wuyts FL, Deelen W, Halley DJ, Oostra BA, Willems PJ. Buyle S, et al. Among authors: reyniers e. Hum Genet. 1993 Oct 1;92(3):269-72. doi: 10.1007/BF00244471. Hum Genet. 1993. PMID: 8406435

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