المؤلفون: Patrick Shannon, Rosanna Weksberg, Ioana Miron, Kathelijne Keymolen, Jean Mathieu, Zuzana Musova, Arturo Lopez-Castel, Julie Letourneau, Michael D. Wilson, Claudia Spits, Sanaa Choufani, Minggao Liang, Silvie Franck, Stéphanie Tomé, Cynthia Gagnon, Stella Lanni, Christopher E. Pearson, David Chitayat, Sara Seneca, Karen Sermon, Lise Barbé, Zdenek Sedlacek

المساهمون: Faculty of Medicine and Pharmacy, Basic (bio-) Medical Sciences, Reproduction and Genetics, Clinical sciences

المصدر: The American Journal of Human Genetics. 100:488-505

مصطلحات موضوعية: Male, 0301 basic medicine, pre-natal diagnosis, Human Embryonic Stem Cells, 0302 clinical medicine, Pregnancy, Myotonic Dystrophy, Genetics(clinical), Child, Promoter Regions, Genetic, Genetics (clinical), Genetics, Myotonin-protein kinase, Methylation, Pedigree, medicine.anatomical_structure, CpG site, DNA methylation, Chorionic villi, Female, SIX5/DMAHP, DMPK, Adult, Adolescent, congenital myotonic dystrophy, parent-of-origin effect(s), Biology, Myotonic dystrophy, Myotonin-Protein Kinase, Article, Cell Line, DNA/CpG methylation, Young Adult, 03 medical and health sciences, medicine, Humans, Epigenetics, epigenetics, Base Sequence, maternal transmission/maternal inheritance, Sequence Analysis, DNA, DNA Methylation, medicine.disease, 030104 developmental biology, Linear Models, CpG Islands, trinucleotide instability, Age of onset, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9d04fdc4968a551c425e61e4245e62c
https://doi.org/10.1016/j.ajhg.2017.01.033