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المؤلفون: Camille Dion, Stéphane Roche, Camille Laberthonnière, Natacha Broucqsault, Virginie Mariot, Shifeng Xue, Alexandra D Gurzau, Agnieszka Nowak, Christopher T Gordon, Marie-Cécile Gaillard, Claire El-Yazidi, Morgane Thomas, Andrée Schlupp-Robaglia, Chantal Missirian, Valérie Malan, Liham Ratbi, Abdelaziz Sefiani, Bernd Wollnik, Bernard Binetruy, Emmanuelle Salort Campana, Shahram Attarian, Rafa
المصدر: Nucleic Acids Research
URL الوصول: https://explore.openaire.eu/search/publication?articleId=r3c4b2081b22::695ed91050c08f577800232398c4d599
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2دورية أكاديمية
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المساهمون: Reversade, Bruno, Dion, Camille, Roche, Stephane, Laberthonniere, Camille, Broucqsault, Natacha, Mariot, Virginie, Xue, Shifeng, Gurzau, Alexandra D., Nowak, Agnieszka, Gordon, Christopher T., Gaillard, Marie-Cecile, El-Yazidi, Claire, Thomas, Morgane, Schlupp-Robaglia, Andree, Missirian, Chantal, Malan, Valerie, Ratbi, Liham, Sefiani, Abdelaziz, Wollnik, Bernd, Binetruy, Bernard, Campana, Emmanuelle Salort, Attarian, Shahram, Bernard, Rafaelle, Nguyen, Karine, Amie, Jeanne, Dumonceaux, Julie, Murphy, James M., Dejardin, Jerome, Blewitt, Marnie E., Robin, Jerome D., Magdinier, Frederique, School of Medicine, Department of Medical Genetics
المصدر: Nucleic Acids Research
مصطلحات موضوعية: Medicine, Biochemistry and molecular biology, Facioscapulohumeral muscular-dystrophy, Pluripotent stem-cells, Inactıve X-chromosome, Gene, Family, Hypomethylation, Mutations, Chromatin, Arhinia, Adopts
وصف الملف: pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3076::2b3e2e71b8f78d9d0ed4afde45d6d90e
http://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/8309
