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American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.
Handchirurgie, Mikrochirurgie, Plastische Chirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse : Organ Der V|July 1, 1996
Genetic aspects of polydactylyJ Zguricas, P Heutink, L Heredero, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 30, 2005
A reduced number of metabotropic glutamate subtype 5 receptors are associated with constitutive homer proteins in a mouse model of fragile X syndromeRaffaella Giuffrida, Sebastiano Musumeci, Simona D'Antoni, et al.
Psychoneuroendocrinology|May 13, 2008
Altered hypothalamus-pituitary-adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndromeJ R Brouwer, E Severijnen, F H de Jong, et al.
Parkinsonism & Related Disorders|October 27, 2006
LRRK2 mutations and Parkinson's disease in Sardinia--A Mediterranean genetic isolateGiovanni Cossu, Marina van Doeselaar, Marcello Deriu, et al.
Neurogenetics|May 16, 2007
The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer's diseaseAlejandro Arias-Vásquez, Aaron Isaacs, Yurii S Aulchenko, et al.
Behavioural Brain Research|May 7, 2005
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS)Debby Van Dam, Vanessa Errijgers, R Frank Kooy, et al.
Genomics|March 1, 1992
Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31M H Koken, E M Smit, I Jaspers-Dekker, et al.
Neurobiology of Disease|December 4, 2002
BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampusMaija Castrén, Katariina E Lampinen, Riitta Miettinen, et al.
Journal of Medical Genetics|June 14, 2008
Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family studyP Henneman, Y S Aulchenko, R R Frants, et al.
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