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Experimental Neurology|September 24, 2004
Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cellsMariëtte Schrier, Lies-Anne Severijnen, Surya Reis, et al.American Journal of Human Genetics|January 1, 1990
Adult and infantile glycogenosis type II in one family, explained by allelic diversityL H Hoefsloot, A T van der Ploeg, M A Kroos, et al.Plos One|January 6, 2010
Association between type 2 diabetes loci and measures of fatnessSlavica Pecioska, M Carola Zillikens, Peter Henneman, et al.Proceedings of the National Academy of Sciences of the United States of America|November 30, 2005
Altered differentiation of neural stem cells in fragile X syndromeMaija Castrén, Topi Tervonen, Virve Kärkkäinen, et al.Child: Care, Health and Development|October 5, 2006
Visual contribution to walking in children with Developmental Coordination DisorderF J A Deconinck, D De Clercq, G J P Savelsbergh, et al.Hormone Research in Paediatrics|September 17, 2011
Genetic variation in candidate genes like the HMGA2 gene in the extremely tallA E J Hendriks, M R Brown, A M Boot, et al.Human Molecular Genetics|March 1, 1997
FMR2 expression in families with FRAXE mental retardationJ Gécz, B A Oostra, A Hockey, et al.Nederlands Tijdschrift Voor Geneeskunde|January 16, 1999
[A large-scale diagnostic program for the fragile X syndrome among the mentally handicapped. I. An epidemiologic survey]L B de Vries, A M van den Ouweland, S Mohkamsing, et al.Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.Journal of Affective Disorders|August 14, 2009
Shared genetic factors in the co-occurrence of symptoms of depression and cardiovascular risk factorsSandra López-León, Yurii S Aulchenko, Henning Tiemeier, et al.Pageof 51