Theresa Mihalic Mosher

Years Active: 2018-2019
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Theresa Mihalic Mosher, Deborah A Zygmunt, Daniel C Koboldt, Benjamin J Kelly, Lisa R Johnson, David S McKenna, Benjamin C Hood, Scott E Hickey, Peter White, Richard K Wilson, Paul T Martin, Kim L McBride
Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasia. European journal of human genetics : EJHG 27 (10) (2019)
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, Ute Grasshoff, Bas de Hoon, Michael Field, Sylvie Manouvrier-Hanu, Scott E Hickey, Molka Kammoun, Karen W Gripp, Claudia Bauer, Christopher Schroeder, Annick Toutain, Theresa Mihalic Mosher, Benjamin J Kelly, Peter White, Andreas Dufke, Eveline Rentmeester, Sungjin Moon, Daniel C Koboldt, Kees E P van Roozendaal, Hao Hu, Stefan A Haas, Hans-Hilger Ropers, Lucinda Murray, Eric A Haan, Marie Shaw, Renee Carroll, Kathryn Friend, Jan Liebelt, Lynne Hobson, Marjan De Rademaeker, Joep Geraedts, Jean-Pierre Fryns, Joris Vermeesch, Martine Raynaud, Olaf Riess, Joost Gribnau, Nicholas Katsanis, Koen Devriendt, Peter Bauer, Jozef Gecz, Christelle Golzio, Cristina Gontan, Vera M Kalscheuer
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder. Molecular psychiatry 24 (11) (2018)

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