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	1.	Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome. [electronic resource] by Storm, K Handig, I Reyniers, E Oostra, B A Kooy, R F Willems, P J Producer: 19980303 In: Human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	An EcoRI RFLP in the 5' region of the human NF1 gene. [electronic resource] by Reyniers, E De Boulle, K Marchuk, D A Andersen, L B Collins, F S Willems, P J Producer: 19940121 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Severe mental retardation and macroorchidism without mutation in the FMR1 gene. [electronic resource] by Reyniers, E Wolff, G Tariverdian, G De Boulle, K Storm, K Kooy, R F 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)
	4.	Apparent regression of the CGG repeat in FMR1 to an allele of normal size. [electronic resource] by Vits, L De Boulle, K Reyniers, E Handig, I Darby, J K Oostra, B Willems, P J Producer: 19941215 In: Human genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Gene conversion between red and defective green opsin gene in blue cone monochromacy. [electronic resource] by Reyniers, E Van Thienen, M N Meire, F De Boulle, K Devries, K Kestelijn, P Willems, P J Producer: 19960807 In: Genomics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11. [electronic resource] by Reyniers, E Van Bogaert, P Peeters, N Vits, L Pauly, F Fransen, E Van Regemorter, N Kooy, R F Producer: 19991210 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type I syndrome. [electronic resource] by Beckers, A Abs, R Reyniers, E De Boulle, K Stevenaert, A Heller, F R Klöppel, G Meurisse, M Willems, P J Producer: 19941221 In: The Journal of clinical endocrinology and metabolism vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Restoring the phenotype of fragile X syndrome: insight from the mouse model. [electronic resource] by Gantois, I Bakker, C E Reyniers, E Willemsen, R D'Hooge, R De Deyn, P P Oostra, B A Kooy, R F Producer: 20020506 In: Current molecular medicine vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mean corpuscular hemoglobin is not increased in Fmr1 knockout mice. [electronic resource] by Reyniers, E Van Bockstaele, D R De Boulle, K Kooy, R F Bakker, C E Oostra, B A Willems, P J Producer: 19960223 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Segregation of the fragile X mutation from an affected male to his normal daughter. [electronic resource] by Willems, P J Van Roy, B De Boulle, K Vits, L Reyniers, E Beck, O Dumon, J E Verkerk, A Oostra, B Producer: 19930831 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging. [electronic resource] by Kooy, R F Reyniers, E Verhoye, M Sijbers, J Bakker, C E Oostra, B A Willems, P J Van Der Linden, A Producer: 19991019 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. [electronic resource] by Vits, L Van Camp, G Coucke, P Fransen, E De Boulle, K Reyniers, E Korn, B Poustka, A Wilson, G Schrander-Stumpel, C Producer: 19941117 In: Nature genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Postmortem examination of two fragile X brothers with an FMR1 full mutation. [electronic resource] by Reyniers, E Martin, J J Cras, P Van Marck, E Handig, I Jorens, H Z Oostra, B A Kooy, R F Willems, P J Producer: 19990624 In: American journal of medical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice. [electronic resource] by Van Dam, D D'Hooge, R Hauben, E Reyniers, E Gantois, I Bakker, C E Oostra, B A Kooy, R F De Deyn, P P Producer: 20010208 In: Behavioural brain research vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Founder effect in a Belgian-Dutch fragile X population. [electronic resource] by Buyle, S Reyniers, E Vits, L De Boulle, K Handig, I Wuyts, F L Deelen, W Halley, D J Oostra, B A Willems, P J Producer: 19931117 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation. [electronic resource] by Kooy, R F Reyniers, E Storm, K Vits, L van Velzen, D de Ruiter, P E Brinkmann, A O de Paepe, A Willems, P J Producer: 20000517 In: American journal of medical genetics vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	17.	Mildly impaired water maze performance in male Fmr1 knockout mice. [electronic resource] by D'Hooge, R Nagels, G Franck, F Bakker, C E Reyniers, E Storm, K Kooy, R F Oostra, B A Willems, P J De Deyn, P P Producer: 19970429 In: Neuroscience vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Long-term potentiation in the hippocampus of fragile X knockout mice. [electronic resource] by Godfraind, J M Reyniers, E De Boulle, K D'Hooge, R De Deyn, P P Bakker, C E Oostra, B A Kooy, R F 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)
	19.	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: 19930702 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. [electronic resource] by Reyniers, E Vits, L De Boulle, K Van Roy, B Van Velzen, D de Graaff, E Verkerk, A J Jorens, H Z Darby, J K Oostra, B Producer: 19930916 In: Nature genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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