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	21.	Alternative splicing in the fragile X gene FMR1. [electronic resource] by Verkerk, A J de Graaff, E De Boulle, K Eichler, E E Konecki, D S Reyniers, E Manca, A Poustka, A Willems, P J Nelson, D L Producer: 19931105 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	A point mutation in the FMR-1 gene associated with fragile X mental retardation. [electronic resource] by De Boulle, K Verkerk, A J Reyniers, E Vits, L Hendrickx, J Van Roy, B Van den Bos, F de Graaff, E Oostra, B A Willems, P J Producer: 19930611 In: Nature genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11. [electronic resource] by Wuyts, W Ramlakhan, S Van Hul, W Hecht, J T van den Ouweland, A M Raskind, W H Hofstede, F C Reyniers, E Wells, D E de Vries, B Producer: 19951012 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	24.	Transgenic mouse model for the fragile X syndrome. [electronic resource] by Kooy, R F D'Hooge, R Reyniers, E Bakker, C E Nagels, G De Boulle, K Storm, K Clincke, G De Deyn, P P Oostra, B A Willems, P J Producer: 19961213 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. [electronic resource] by Wu, Y Q Heutink, P de Vries, B B Sandkuijl, L A van den Ouweland, A M Niermeijer, M F Galjaard, H Reyniers, E Willems, P J Halley, D J Producer: 19940523 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics. [electronic resource] by Rooms, L Reyniers, E Wuyts, W Storm, K van Luijk, R Scheers, S Wauters, J van den Ende, J Biervliet, M Eyskens, F van Goethem, G Laridon, A Ceulemans, B Courtens, W Kooy, R F Producer: 20060612 In: Clinical genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3). [electronic resource] by Holinski-Feder, E Reyniers, E Uhrig, S Golla, A Wauters, J Kroisel, P Bossuyt, P Rost, I Jedele, K Zierler, H Schwab, S Wildenauer, D Speicher, M R Willems, P J Meitinger, T Kooy, R F Producer: 20000309 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. [electronic resource] by Fransen, E D'Hooge, R Van Camp, G Verhoye, M Sijbers, J Reyniers, E Soriano, P Kamiguchi, H Willemsen, R Koekkoek, S K De Zeeuw, C I De Deyn, P P Van der Linden, A Lemmon, V Kooy, R F Willems, P J Producer: 19980619 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Positional cloning of a gene involved in hereditary multiple exostoses. [electronic resource] by Wuyts, W Van Hul, W Wauters, J Nemtsova, M Reyniers, E Van Hul, E V De Boulle, K de Vries, B B Hendrickx, J Herrygers, I Bossuyt, P Balemans, W Fransen, E Vits, L Coucke, P Nowak, N J Shows, T B Mallet, L van den Ouweland, A M McGaughran, J Halley, D J Willems, P J Producer: 19970204 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency. [electronic resource] by Guergueltcheva, V Peeters, K Baets, J Ceuterick-de Groote, C Martin, J J Suls, A De Vriendt, E Mihaylova, V Chamova, T Almeida-Souza, L Ydens, E Tzekov, C Hadjidekov, G Gospodinova, M Storm, K Reyniers, E Bichev, S van der Ven, P F M Fürst, D O Mitev, V Lochmüller, H Timmerman, V Tournev, I De Jonghe, P Jordanova, A Producer: 20120209 In: Neurology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)