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Journal of Medical Genetics|September 3, 2004
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)J Ramser, B Winnepenninckx, C Lenski, et al.Human Genetics|June 1, 1993
Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13R F Kooy, A Y Van der Veen, E Verlind, et al.Nucleic Acids Research|December 11, 1991
The Trypanosoma brucei DNA polymerase alpha core subunit gene is developmentally regulated and linked to a constitutively expressed open reading frameP A Leegwater, M Strating, N B Murphy, et al.Acta Tropica|February 1, 1990
Influence of fever and flurbiprofen on trypanosome growthD Zwart, R Brun, R H Dwinger, et al.American Journal of Human Genetics|October 16, 1999
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11E Reyniers, P Van Bogaert, N Peeters, et al.Current Molecular Medicine|March 20, 2002
Restoring the phenotype of fragile X syndrome: insight from the mouse modelI Gantois, C E Bakker, E Reyniers, et al.Current Biology : CB|January 4, 2001
Long-term potentiation in mice lacking the neural cell adhesion molecule L1T Bliss, M Errington, E Fransen, et al.Behavioural Brain Research|April 16, 2017
Behavioural characterization of AnkyrinG deficient mice, a model for ANK3 related disordersI M van der Werf, D Van Dam, S Missault, et al.Human Genetics|January 1, 1996
Mean corpuscular hemoglobin is not increased in Fmr1 knockout miceE Reyniers, D R Van Bockstaele, K De Boulle, et al.European Journal of Human Genetics : EJHG|August 10, 1999
Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imagingR F Kooy, E Reyniers, M Verhoye, et al.Pageof 4