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Page 1
Positional cloning of a gene involved in hereditary multiple exostoses.
Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ. Wuyts W, et al. Among authors: willems pj. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
Wessels MW, De Graaf BM, Cohen-Overbeek TE, Spitaels SE, de Groot-de Laat LE, Ten Cate FJ, Frohn-Mulder IF, de Krijger R, Bartelings MM, Essed N, Wladimiroff JW, Niermeijer MF, Heutink P, Oostra BA, Dooijes D, Bertoli-Avella AM, Willems PJ. Wessels MW, et al. Among authors: willems pj. Hum Genet. 2008 Jan;122(6):595-603. doi: 10.1007/s00439-007-0436-x. Epub 2007 Oct 16. Hum Genet. 2008. PMID: 17938964
Characterization of FMR1 proteins isolated from different tissues.
Verheij C, de Graaff E, Bakker CE, Willemsen R, Willems PJ, Meijer N, Galjaard H, Reuser AJ, Oostra BA, Hoogeveen AT. Verheij C, et al. Among authors: willems pj. Hum Mol Genet. 1995 May;4(5):895-901. doi: 10.1093/hmg/4.5.895. Hum Mol Genet. 1995. PMID: 7633450
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. Among authors: willems pj. Hum Genet. 1993 Dec;92(6):631. doi: 10.1007/BF00420953. Hum Genet. 1993. PMID: 7903272 Free article.
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: willems pj. Hum Genet. 1993 Oct 1;92(3):269-72. doi: 10.1007/BF00244471. Hum Genet. 1993. PMID: 8406435
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: willems pj. Hum Mol Genet. 1993 Apr;2(4):399-404. doi: 10.1093/hmg/2.4.399. Hum Mol Genet. 1993. PMID: 8504300
FMRP is associated to the ribosomes via RNA.
Tamanini F, Meijer N, Verheij C, Willems PJ, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: willems pj. Hum Mol Genet. 1996 Jun;5(6):809-13. doi: 10.1093/hmg/5.6.809. Hum Mol Genet. 1996. PMID: 8776596
Angelman syndrome in an inbred family.
Beuten J, Hennekam RC, Van Roy B, Mangelschots K, Sutcliffe JS, Halley DJ, Hennekam FA, Beaudet AL, Willems PJ. Beuten J, et al. Among authors: willems pj. Hum Genet. 1996 Mar;97(3):294-8. doi: 10.1007/BF02185757. Hum Genet. 1996. PMID: 8786067 Free article.
Noninvasive test for fragile X syndrome, using hair root analysis.
Willemsen R, Anar B, De Diego Otero Y, de Vries BB, Hilhorst-Hofstee Y, Smits A, van Looveren E, Willems PJ, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: willems pj. Am J Hum Genet. 1999 Jul;65(1):98-103. doi: 10.1086/302462. Am J Hum Genet. 1999. PMID: 10364521 Free PMC article.
257 results