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 |