학술논문
Identification of DNA methylation episignature for the intellectual developmental disorder, autosomal dominant 21 syndrome, caused by variants in the CTCF gene
Document Type
Article
Author
Karimi, K.; Haghshenas, S.; Relator, R.; Levy, M.A.; Kerkhof, J.; McConkey, H.; Sadikovic, B.; Mol, M.O.; Brooks, A.; Bouman, A.; Zonneveld-Huijssoon, E.; Gerkes, E.H.; Tedder, M.L.; Vissers, L.; Salzano, E.; Piccione, M.; Asaftei, S.D.; Carli, D.; Trajkova, S.; Brusco, A.; Mussa, A.; Shukarova-Angelovska, E.; Merla, G.; Alders, M.M.
Source
In: Genetics in Medicine . (Genetics in Medicine, March 2024, 26(3))
Subject
Language
English
ISSN
15300366
10983600
10983600