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American Journal of Medical Genetics|July 31, 1995
Trisomy 1q42 --> qter in a sister and brother: further delineation of the "trisomy 1q42 --> qter syndrome"C C Verschuuren-Bemelmans, B Leegte, T M Hodenius, et al.Prenatal Diagnosis|December 13, 2000
Four years' cytogenetic experience with the culture of chorionic villiB Sikkema-Raddatz, K Bouman, C C Verschuuren-Bemelmans, et al.Prenatal Diagnosis|October 4, 2000
Trends in live birth prevalence of down syndrome in the Northern Netherlands 1987-96: the impact of screening and prenatal diagnosisM J Wortelboer, B T De Wolf, C C Verschuuren-Bemelmans, et al.Neurology|September 28, 2005
Striatal dopamine D2 receptors, metabolism, and volume in preclinical Huntington diseaseJ C H van Oostrom, R P Maguire, C C Verschuuren-Bemelmans, et al.Journal of Medical Genetics|December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic studyK L Greenhalgh, R T Howell, A Bottani, et al.Human Genetics|December 1, 1995
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.Early Human Development|September 25, 2009
Neurophysiological evaluation in children with Friedreich's ataxiaD A Sival, G J du Marchie Sarvaas, O F Brouwer, et al.Neurology|March 13, 2002
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysisB P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, et al.European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.Pageof 2