Erratum: De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias (Genetics in Medicine (2023) 25(10), (S1098360023009401), (10.1016/j.gim.2023.100927))

Publication date

2023-11

Authors

Harms, Frederike L.
Dingemans, Alexander J.M.
Hempel, Maja
Pfundt, Rolph
Bierhals, Tatjana
Casar, Christian
Müller, Christian
Niermeijer, Jikke Mien F.
Fischer, Jan
Jahn, Arne

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Abstract

Correction to: Genetics in Medicine 2023; https://doi.org/10.1016/j.gim.2023.100927, published online 6 July 2023. In the article “De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias” (Genet Med 2023;25:100927), the following update was made. In the author listing, the author's name “Tahshin S. Barakat” has been updated to “Tahsin Stefan Barakat.” Please see revised author listing shown above. The article has been corrected online can be accessed at https://doi.org/10.1016/j.gim.2023.100927.

Keywords

Taverne, Genetics(clinical)

Citation

Harms, F L, Dingemans, A J M, Hempel, M, Pfundt, R, Bierhals, T, Casar, C, Müller, C, Niermeijer, J M F, Fischer, J, Jahn, A, Hübner, C, Majore, S, Agolini, E, Novelli, A, van der Smagt, J, Ernst, R, van Binsbergen, E, Mancini, G M S, van Slegtenhorst, M, Barakat, T S, Wakeling, E L, Kamath, A, Downie, L, Pais, L, White, S M, de Vries, B B A & Kutsche, K 2023, 'Erratum : De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias (Genetics in Medicine (2023) 25(10), (S1098360023009401), (10.1016/j.gim.2023.100927))', Genetics in Medicine, vol. 25, no. 11, 100964. https://doi.org/10.1016/j.gim.2023.100964