Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

The Original Article was published on 07 August 2019

Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019

In the original version of this Article the author Solveig Heide was incorrectly given as Heide Solveig. There was also an error in the spelling of the author Sandra Whalen, which was given as Sandra Wallen. In addition, the affiliation for Sandra Whalen was mistakenly quoted as AP-HP, Département de Génétique, Centre de Référence Maladies Rares “Anomalies du développement et syndromes malformatifs” Hôpital de la Pitié Salpêtrière, Paris, France instead of UF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France. All errors are now corrected in both the PDF and HTML versions of the Article.

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Correspondence to Karin Weiss MD.

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Weiss, K., Lazar, H.P., Kurolap, A. et al. Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis. Genet Med 22, 669 (2020). https://doi.org/10.1038/s41436-019-0727-3

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