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Journal of Medical Genetics|September 3, 2009
Fragile X syndrome: from molecular genetics to therapyC D'Hulst, R F KooyCytogenetic and Genome Research|July 9, 2004
Genetic modifiers in mice: the example of the fragile X mouse modelV Errijgers, R F KooyMolecular Medicine Today|April 27, 2000
Fragile X syndrome at the turn of the centuryR F Kooy, R Willemsen, B A OostraEuropean Journal of Human Genetics : EJHG|April 21, 2001
Brain studies of mouse models for neurogenetic disorders using in vivo magnetic resonance imaging (MRI)R F Kooy, M Verhoye, V Lemmon, et al.European Journal of Human Genetics : EJHG|January 1, 1995
An integrated map of human chromosome 13 allowing regional localization of genetic markersR F Kooy, A Wijngaard, E Verlind, et al.Genomics|December 10, 1995
A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemiaL Hawthorn, T Roberts, E Verlind, et al.Molecular and Biochemical Parasitology|August 1, 1989
On the DNA content of Trypanosoma cruziR F Kooy, F Ashall, M Van der Ploeg, et al.Human Genetics|March 7, 1998
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndromeK Storm, I Handig, E Reyniers, et al.Clinical Genetics|August 2, 2014
Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencingC Helsmoortel, G Vandeweyer, P Ordoukhanian, et al.American Journal of Medical Genetics|August 9, 1996
Severe mental retardation and macroorchidism without mutation in the FMR1 geneE Reyniers, G Wolff, G Tariverdian, et al.Pageof 4