دورية أكاديمية

EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome

التفاصيل البيبلوغرافية
العنوان: EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome
المؤلفون: Goodman, Sarah J., Cytrynbaum, Cheryl, Chung, Brian Hon-Yin, Chater-Diehl, Eric, Aziz, Celine, Turinsky, Andrei L., Kellam, Barbara, Keller, Melanie, Ko, Jung Min, Caluseriu, Oana, Grafodatskaya, Daria, McCready, Elizabeth, Perrier, Renee, Yeung, Kit San, Ho-Ming, Luk, Machado, Jerry, Brudno, Michael, Stavropoulos, D. James, Scherer, Stephen W., Innes, A. Micheil, Cheung, Sau Wei, Choufani, Sanaa, Weksberg, Rosanna
المساهمون: Canadian Institutes of Health Research (CIHR), The Lymphoma and Leukemia Society of Canada, the Canadian Centre for Computational Genomics (C3G), the Genome Technology Platform (GTP), Genome Canada through Genome Quebec and Ontario Genomics (AL Turinsky, M Brudno), Genome Canada through Ontario Genomics (AL Turinsky, M Brudno and R Weksberg), Health and Medical Research Fund, the Society of Relief for Disabled Children of Hong Kong (SRDC)
المصدر: Journal of Translational Genetics and Genomics
بيانات النشر: OAE Publishing Inc.
سنة النشر: 2020
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
DOI: 10.20517/jtgg.2020.23
الإتاحة: https://doi.org/10.20517/jtgg.2020.23Test
رقم الانضمام: edsbas.93FD5227
قاعدة البيانات: BASE