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المؤلفون: Johanne M. Groothuismink, Manon Damen, Mascha M.V.A.P. Schijvenaars, Marlies Schimmel-Naber, A.A. Tieleman, Marieke J H Coenen
المصدر: Journal of Neuromuscular Diseases, 8, 715-722
Journal of Neuromuscular Diseases, 8, 4, pp. 715-722مصطلحات موضوعية: 0301 basic medicine, Adult, Male, India, Single-nucleotide polymorphism, 030105 genetics & heredity, Biology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, Genetic variation, SNP, Humans, Myotonic Dystrophy, Gene, Aged, Netherlands, Genetics, Suriname, Portugal, Haplotype, Intron, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Morocco, Neurology, Haplotypes, Inflammatory diseases Radboud Institute for Health Sciences [Radboudumc 5], Microsatellite, Female, Neurology (clinical), Trinucleotide repeat expansion, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6129650892a4acf407400b9ea40a10d8Test
https://hdl.handle.net/2066/236726Test -
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المؤلفون: William Howlett, H.A. van Duyvenvoorde, A.A. Tieleman, O.J. Igogo, Marieke C. J. Dekker, Ben C.J. Hamel
المصدر: Neuromuscular Disorders, 29, 317-320
Neuromuscular Disorders, 29, 4, pp. 317-320
Neuromuscular Disorders, 29(4), 317-320. PERGAMON-ELSEVIER SCIENCE LTDمصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, medicine.medical_specialty, Weakness, Other Research Donders Center for Medical Neuroscience [Radboudumc 0], Global neurology, Muscle disorder, Medical care, Tanzania, 03 medical and health sciences, 0302 clinical medicine, Genotype, parasitic diseases, Medicine, Humans, Muscular dystrophy, Genetics (clinical), biology, business.industry, Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], biology.organism_classification, medicine.disease, Pedigree, Muscular Dystrophy, Duchenne, 030104 developmental biology, Neurology, Becker muscular dystrophy, Pediatrics, Perinatology and Child Health, Africa, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0752a7384cf77838f3b6b66d836efc0Test
http://hdl.handle.net/2066/207145Test -
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المؤلفون: Mascha M.V.A.P. Schijvenaars, Baziel G.M. van Engelen, A.A. Tieleman, Laura P.W. Ranum, Marieke J H Coenen, Maike Leferink, Hans Scheffer
المصدر: European Journal of Human Genetics, 19, 5, pp. 567-70
European Journal of Human Genetics, 19, 567-70مصطلحات موضوعية: musculoskeletal diseases, Population, Functional Neurogenomics Human Movement & Fatigue [DCN 2], Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Biology, Myotonic dystrophy, Polymorphism, Single Nucleotide, Article, Polymorphism (computer science), Genetics, medicine, Humans, Myotonic Dystrophy, Allele, education, Genomic disorders and inherited multi-system disorders Molecular epidemiology [IGMD 3], Genetics (clinical), Netherlands, education.field_of_study, Haplotype, RNA-Binding Proteins, medicine.disease, Founder Effect, Morocco, Haplotypes, Microsatellite, Trinucleotide repeat expansion, Founder effect, Myotonic Disorders
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9665d6336bad3899b727c970cacb4602Test
https://hdl.handle.net/2066/96834Test