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American Journal of Human Genetics|March 21, 2000
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutationsR D Hundscheid, E A Sistermans, C M Thomas, et al.Neurobiology of Learning and Memory|March 5, 2011
Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO miceJosien Levenga, Femke M S de Vrij, Ronald A M Buijsen, et al.Journal of Medical Genetics|April 16, 1999
Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacitiesA T Helderman-van den Enden, P D Maaswinkel-Mooij, E Hoogendoorn, et al.American Journal of Medical Genetics|August 9, 1996
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cellsE de Graaff, B B de Vries, R Willemsen, et al.Human Genetics|August 1, 1991
Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13J F De Rijk-van Andel, C E Catsman-Berrevoets, D J Halley, et al.BJOG : an International Journal of Obstetrics and Gynaecology|February 4, 2009
Body composition by dual-energy X-ray absorptiometry in women with previous pre-eclampsia or small-for-gestational-age offspringA L Berends, M C Zillikens, C J M de Groot, et al.American Journal of Medical Genetics|May 20, 1999
Postmortem examination of two fragile X brothers with an FMR1 full mutationE Reyniers, J J Martin, P Cras, et al.Behavioural Brain Research|December 2, 2000
Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout miceD Van Dam, R D'Hooge, E Hauben, et al.Diabetologia|February 9, 2006
Heritability of fasting glucose levels in a young genetically isolated populationR L P Santos, M C Zillikens, F R Rivadeneira, et al.Neurology|June 1, 1997
Apolipoprotein E gene and sporadic frontal lobe dementiaM Stevens, C M van Duijn, P de Knijff, et al.Pageof 51