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Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.American Journal of Medical Genetics. Part A|August 21, 2007
ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphomaC Schuetz, G Barbi, T F E Barth, et al.Neuromuscular Disorders : NMD|September 29, 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophyE L van der Kooi, J C de Greef, M Wohlgemuth, et al.Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.Journal of Medical Genetics|September 26, 2007
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)M M Hagleitner, A Lankester, P Maraschio, et al.Pageof 1