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Psychiatric Genetics|April 29, 2009
High activity of monoamine oxidase A is associated with externalizing behaviour in maltreated and nonmaltreated adopteesEsther J M van der Vegt, Ben A Oostra, Alejandro Arias-Vásquez, et al.
The Journal of Experimental Biology|August 4, 2009
Reduction in fragile X related 1 protein causes cardiomyopathy and muscular dystrophy in zebrafishSandra Van't Padje, Bill Chaudhry, Lies-Anne Severijnen, et al.
Genes and Immunity|August 24, 2012
Decreased systemic IL-7 and soluble IL-7Rα in multiple sclerosis patientsK L Kreft, E Verbraak, A F Wierenga-Wolf, 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.
Early Human Development|May 15, 2023
Neurodevelopmental outcome in children with congenital cytomegalovirus infection: A prospective multicenter cohort studyA Keymeulen, E De Leenheer, A Casaer, et al.
Genes and Immunity|April 11, 2008
EVI5 is a risk gene for multiple sclerosisI A Hoppenbrouwers, Y S Aulchenko, G C Ebers, et al.
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
BMC Medicine|October 18, 2008
Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort studyAbbas Dehghan, Mandy van Hoek, Eric J G Sijbrands, et al.
American Journal of Medical Genetics|July 15, 1994
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndromeP Chiurazzi, E de Graaff, J Ng, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Brachydactyly and short stature in a kindred with early-onset parkinsonismMarieke C J Dekker, R J H Galjaard, P J L M Snijders, et al.
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