المؤلفون: Silvère M. van der Maarel, Pilar Camaño, George W. Padberg, Gert-Jan B. van Ommen, Patrick J. van der Vliet, Johannes G. Dauwerse, Daniel G. Miller, Richard J.L.F. Lemmers, Rune R. Frants, Rinse Klooster, Kirsten R. Straasheijm, Stephen J. Tapscott, Rabi Tawil, Lauren Snider, Sabrina Sacconi

المصدر: Science, 329(5999), 1650-1653
Science
Science, 329, 1650-3
Science, 329, 5999, pp. 1650-3

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Transcription, Genetic, RNA Stability, Molecular Sequence Data, Biology, Transfection, Polyadenylation, Polymorphism, Single Nucleotide, Article, Young Adult, DUX4, Genetic model, medicine, Humans, Facioscapulohumeral muscular dystrophy, Genetic Predisposition to Disease, RNA, Messenger, Muscular dystrophy, Alleles, dna rearrangements fshd rna 4q d4z4, Aged, Repetitive Sequences, Nucleic Acid, Homeodomain Proteins, Genetics, Multidisciplinary, Base Sequence, Models, Genetic, Chromosomes, Human, Pair 10, Haplotype, Chromosome, Middle Aged, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, Haplotypes, Child, Preschool, Chromosomal region, Homeobox, Female, Chromosomes, Human, Pair 4, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60d0d5fc0fa1eac699bb94eb6c627396Test
https://doi.org/10.1126Test/science.1189044

المؤلفون: Lemmers, R.J.L.F., Vliet, P.J. van der, Klooster, R., Sacconi, S., Camano, P., Dauwerse, J.G., Snider, L., Straasheijm, K.R., Ommen, G.J. van, Padberg, G.W., Miller, D.G., Tapscott, S.J., Tawil, R., Frants, R.R., Maarel, S.M. van der

المصدر: Science

مصطلحات موضوعية: dna rearrangements fshd rna 4q d4z4

العلاقة: lumc-id: 4414012; https://hdl.handle.net/1887/108534Test

الإتاحة: https://doi.org/10.1126Test/science.1189044
https://hdl.handle.net/1887/108534Test