The CHD4-related Syndrome: a Comprehensive Investigation of the Clinical Spectrum, Genotype-Phenotype Correlations, and Molecular Basis (vol 17, Pg 189, 2019) Karin Weiss , Hayley P. Lazar , Alina Kurolap , Ariel F. Martinez , Tamar Paperna , Lior Cohen , Marie F. Smeland , Sandra Whalen , Solveig Heide , Boris Keren , Pauline Terhal , Melita Irving , Motoki Takaku , John D. Roberts , Robert M. Petrovich , Samantha A. Schrier Vergano , Amy Kenney , Hanne Hove , Elizabeth DeChene , Shane C. Quinonez , Estelle Colin , Alban Ziegler , Melissa Rumple , Mahim Jain , Danielle Monteil , Elizabeth R. Roeder , Kimberly Nugent , Arie van Haeringen , Michael Gambello , Avni Santani , Livija Medne , Bryan Krock , Cara M. Skraban , Elaine H. Zackai , Holly A. Dubbs , Thomas Smol , Jamal Ghoumid , Michael J. Parker , Michael Wright , Peter Turnpenny , Jill Clayton-Smith , Kay Metcalfe , Hitoshi Kurumizaka , Bruce D. Gelb , Hagit Baris Feldman , Philippe M. Campeau , Maximilian Muenke , Paul A. Wade , Katherine Lachlan GENETICS IN MEDICINE（2020）
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An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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