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))
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; Hübner, Christoph; Majore, Silvia; Agolini, Emanuele; Novelli, Antonio; van der Smagt, Jasper; Ernst, Robert; van Binsbergen, Ellen; Mancini, Grazia M.S.; van Slegtenhorst, Marjon; Barakat, Tahsin Stefan; Wakeling, Emma L.; Kamath, Arveen; Downie, Lilian; Pais, Lynn; White, Susan M.; de Vries, Bert B.A.; Kutsche, Kerstin
(2023) Genetics in Medicine, volume 25, issue 11
(Comment)
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
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“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.
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Keywords: Genetics(clinical)
ISSN: 1098-3600
Publisher: Lippincott Williams & Wilkins
Note: Publisher Copyright: © 2023 American College of Medical Genetics and Genomics
(Peer reviewed)