Comparative study of methyl-CpG-binding domain proteins

por Roloff, Tim C, Ropers, H Hilger, Nuber, Ulrike A
Publicado 2003

CGHPRO – A comprehensive data analysis tool for array CGH

por Chen, Wei, Erdogan, Fikret, Ropers, H-Hilger, Lenzner, Steffen, Ullmann, Reinhard
Publicado 2005

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

por Davarniya, Behzad, Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Hosseini, Masoumeh, Maqsoud, Fariba, Farajollahi, Reza, Wienker, Thomas F., Ropers, H. Hilger, Najmabadi, Hossein
Publicado 2015

BRCA1-mediated repression of select X chromosome genes

por Jazaeri, Amir A, Chandramouli, Gadisetti VR, Aprelikova, Olga, Nuber, Ulrike A, Sotiriou, Christos, Liu, Edison T, Ropers, H Hilger, Yee, Cindy J, Boyd, Jeff, Barrett, J Carl
Publicado 2004

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

por Bainbridge, Matthew N, Hu, Hao, Muzny, Donna M, Musante, Luciana, Lupski, James R, Graham, Brett H, Chen, Wei, Gripp, Karen W, Jenny, Kim, Wienker, Thomas F, Yang, Yaping, Sutton, V Reid, Gibbs, Richard A, Ropers, H Hilger
Publicado 2013

BOD1 Is Required for Cognitive Function in Humans and Drosophila

por Esmaeeli-Nieh, Sahar, Fenckova, Michaela, Porter, Iain M., Motazacker, M. Mahdi, Nijhof, Bonnie, Castells-Nobau, Anna, Asztalos, Zoltan, Weißmann, Robert, Behjati, Farkhondeh, Tzschach, Andreas, Felbor, Ute, Scherthan, Harry, Sayfati, Seyed Morteza, Ropers, H. Hilger., Kahrizi, Kimia, Najmabadi, Hossein, Swedlow, Jason R., Schenck, Annette, Kuss, Andreas W.
Publicado 2016