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))

Frederike L. Harms; Alexander J.M. Dingemans; Maja Hempel; Rolph Pfundt; Tatjana Bierhals; Christian Casar; Christian Müller; Jikke Mien F. Niermeijer; Jan Fischer; Arne Jahn; Christoph Hübner; Silvia Majore; Emanuele Agolini; Antonio Novelli; Jasper van der Smagt; Robert Ernst; Ellen van Binsbergen; Grazia M.S. Mancini; Marjon van Slegtenhorst; Tahsin Stefan Barakat; Emma L. Wakeling; Arveen Kamath; Lilian Downie; Lynn Pais; Susan M. White; Bert B.A. de Vries; Kerstin Kutsche

doi:10.1016/j.gim.2023.100964

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))

Frederike L. Harms
, Alexander J.M. Dingemans
, Maja Hempel
, Rolph Pfundt
, Tatjana Bierhals
, Christian Casar
, Christian Müller
, Jikke Mien F. Niermeijer
, Jan Fischer
, Arne Jahn
, Christoph Hübner
, Silvia Majore
, Emanuele Agolini
, Antonio Novelli
, Jasper van der Smagt
, Robert Ernst
, Ellen van Binsbergen
, Grazia M.S. Mancini
, Marjon van Slegtenhorst
, Tahsin Stefan Barakat

Emma L. Wakeling, Arveen Kamath, Lilian Downie, Lynn Pais, Susan M. White, Bert B.A. de Vries, Kerstin Kutsche

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

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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.

Original language	English
Article number	100964
Journal	Genetics in Medicine
Volume	25
Issue number	11
DOIs	https://doi.org/10.1016/j.gim.2023.100964
Publication status	Published - Nov 2023

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10.1016/j.gim.2023.100964

PIIS1098360023009802Final published version, 315 KBLicence: Taverne

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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., ... 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, 25(11), Article 100964. https://doi.org/10.1016/j.gim.2023.100964

@article{ccc2f37cdfc548c8b3191308add57e18,

title = "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))",

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.",

author = "Harms, \{Frederike L.\} and Dingemans, \{Alexander J.M.\} and Maja Hempel and Rolph Pfundt and Tatjana Bierhals and Christian Casar and Christian M{\"u}ller and Niermeijer, \{Jikke Mien F.\} and Jan Fischer and Arne Jahn and Christoph H{\"u}bner and Silvia Majore and Emanuele Agolini and Antonio Novelli and \{van der Smagt\}, Jasper and Robert Ernst and \{van Binsbergen\}, Ellen and Mancini, \{Grazia M.S.\} and \{van Slegtenhorst\}, Marjon and Barakat, \{Tahsin Stefan\} and Wakeling, \{Emma L.\} and Arveen Kamath and Lilian Downie and Lynn Pais and White, \{Susan M.\} and \{de Vries\}, \{Bert B.A.\} and Kerstin Kutsche",

note = "Publisher Copyright: {\textcopyright} 2023 American College of Medical Genetics and Genomics",

year = "2023",

month = nov,

doi = "10.1016/j.gim.2023.100964",

language = "English",

volume = "25",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier",

number = "11",

}

Harms, FL, Dingemans, AJM, Hempel, M, Pfundt, R, Bierhals, T, Casar, C, Müller, C, Niermeijer, JMF, Fischer, J, Jahn, A, Hübner, C, Majore, S, Agolini, E, Novelli, A, van der Smagt, J , Ernst, R , van Binsbergen, E, Mancini, GMS, van Slegtenhorst, M, Barakat, TS, Wakeling, EL, Kamath, A, Downie, L, Pais, L, White, SM, de Vries, BBA & 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

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 et al.
In: Genetics in Medicine, Vol. 25, No. 11, 100964, 11.2023.

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

TY - JOUR

T1 - Erratum

T2 - 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))

AU - Harms, Frederike L.

AU - Dingemans, Alexander J.M.

AU - Hempel, Maja

AU - Pfundt, Rolph

AU - Bierhals, Tatjana

AU - Casar, Christian

AU - Müller, Christian

AU - Niermeijer, Jikke Mien F.

AU - Fischer, Jan

AU - Jahn, Arne

AU - Hübner, Christoph

AU - Majore, Silvia

AU - Agolini, Emanuele

AU - Novelli, Antonio

AU - van der Smagt, Jasper

AU - Ernst, Robert

AU - van Binsbergen, Ellen

AU - Mancini, Grazia M.S.

AU - van Slegtenhorst, Marjon

AU - Barakat, Tahsin Stefan

AU - Wakeling, Emma L.

AU - Kamath, Arveen

AU - Downie, Lilian

AU - Pais, Lynn

AU - White, Susan M.

AU - de Vries, Bert B.A.

AU - Kutsche, Kerstin

PY - 2023/11

Y1 - 2023/11

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85171593109

U2 - 10.1016/j.gim.2023.100964

DO - 10.1016/j.gim.2023.100964

M3 - Comment/Letter to the editor

C2 - 37728613

AN - SCOPUS:85171593109

SN - 1098-3600

VL - 25

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 11

M1 - 100964

ER -

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))

Abstract

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De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias

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