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Suzanna G M Frints

Years Active: 2019-2019
Publications (10 Years): 1

Maastricht Universitair Medisch Centrum+

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

Affiliation History

Maastricht Universitair Medisch Centrum+ Feb 1o 2003

Netherlands

MD, PhD, Clinical Geneticst, UHD :: Clinical Genetics

Publications

Suzanna G M Frints, Friederike Hennig, Roberto Colombo, Sebastien Jacquemont, Paulien Terhal, Holly H Zimmerman, David Hunt, Bryce A Mendelsohn, Ulrike Kordaß, Richard Webster, Margje Sinnema, Omar Abdul-Rahman, Vanessa Suckow, Alberto Fernández-Jaén, Kees van Roozendaal, Servi J C Stevens, Merryn V E Macville, Salwan Al-Nasiry, Koen van Gassen, Norbert Utzig, Suzanne M Koudijs, Lesley McGregor, Saskia M Maas, Diana Baralle, Abhijit Dixit, Peter Wieacker, Marcus Lee, Arthur S Lee, Elizabeth C Engle, Gunnar Houge, Gyri A Gradek, Andrew G L Douglas, Cheryl Longman, Shelagh Joss, Danita Velasco, Raoul C M Hennekam, Hiromi Hirata, Vera M Kalscheuer
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita. Human mutation 40 (12) (2019)

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