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Clinical Genetics|October 7, 2005
Subtelomeric chromosome aberrations: still a lot to learnU Moog, Y H J M Arens, J C M van Lent-Albrechts, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
The Journal of Physiology|December 3, 2019
Postexercise cooling impairs muscle protein synthesis rates in recreational athletesCas J Fuchs, Imre W K Kouw, Tyler A Churchward-Venne, et al.
Cardiovascular and Interventional Radiology|May 19, 2017
Uterine Artery Embolization for Symptomatic Adenomyosis: 7-Year Clinical Follow-up Using UFS-Qol QuestionnaireAnnefleur M de Bruijn, Marieke Smink, Wouter J K Hehenkamp, et al.
Developmental Cognitive Neuroscience|March 23, 2012
The effect of the OPRM1 and DRD4 polymorphisms on the relation between attentional bias and alcohol use in adolescence and young adulthoodSara Pieters, Haske Van Der Vorst, William J Burk, et al.
JIMD Reports|February 23, 2013
Altered carbon dioxide metabolism and creatine abnormalities in rett syndromeNicky S J Halbach, Eric E J Smeets, Jörgen Bierau, et al.
Neurology|January 27, 1998
A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesI F de Coo, E A Sistermans, I J de Wijs, et al.
Human Molecular Genetics|August 1, 1994
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndromeH H Lemmink, T Mochizuki, L P van den Heuvel, et al.
Annals of the Rheumatic Diseases|February 14, 2004
Activation of the STAT1 pathway in rheumatoid arthritisP V Kasperkovitz, N L Verbeet, T J Smeets, et al.
International Journal of Cancer|May 26, 2010
Immortalization of oral keratinocytes by functional inactivation of the p53 and pRb pathwaysSerge J Smeets, Marlon van der Plas, Tieneke B M Schaaij-Visser, et al.
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