Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation (Genetics in Medicine, (2020), 22, 9, (1498-1506), 10.1038/s41436-020-0817-2)

Genomics England Research Consortium

doi:10.1038/s41436-020-0886-2

Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation (Genetics in Medicine, (2020), 22, 9, (1498-1506), 10.1038/s41436-020-0817-2)

Genomics England Research Consortium

General Pediatrics

Research output: Contribution to journal › Comment/debate

Abstract

The version of the Article previously published did not acknowledge Freya Boardman-Pretty^17,18 and the Genomics England Research Consortium in the author list. This has now been corrected in both the PDF and HTML versions of the Article. ¹⁷Genomics England, London, UK; ¹⁸William Harvey Research Institute, Queen Mary University of London, London, UK

Original language	English (US)
Pages (from-to)	1567
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	9
DOIs	https://doi.org/10.1038/s41436-020-0886-2
State	Published - Sep 1 2020

ASJC Scopus subject areas

Genetics(clinical)

Access to Document

10.1038/s41436-020-0886-2

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Genomics England Research Consortium (2020). Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation (Genetics in Medicine, (2020), 22, 9, (1498-1506), 10.1038/s41436-020-0817-2). Genetics in Medicine, 22(9), 1567. https://doi.org/10.1038/s41436-020-0886-2

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title = "Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation (Genetics in Medicine, (2020), 22, 9, (1498-1506), 10.1038/s41436-020-0817-2)",

abstract = "The version of the Article previously published did not acknowledge Freya Boardman-Pretty17,18 and the Genomics England Research Consortium in the author list. This has now been corrected in both the PDF and HTML versions of the Article. 17Genomics England, London, UK; 18William Harvey Research Institute, Queen Mary University of London, London, UK",

author = "{Genomics England Research Consortium} and Eduardo Calpena and Araceli Cuellar and Krithi Bala and Swagemakers, {Sigrid M.A.} and Nils Koelling and McGowan, {Simon J.} and Phipps, {Julie M.} and Meena Balasubramanian and Cunningham, {Michael L.} and Sofia Douzgou and Wanda Lattanzi and Morton, {Jenny E.V.} and Deborah Shears and Astrid Weber and Wilson, {Louise C.} and Helen Lord and Tracy Lester and David Johnson and Wall, {Steven A.} and Twigg, {Stephen R.F.} and Mathijssen, {Irene M.J.} and Freya Boardman-Pretty and Boyadjiev, {Simeon A.} and Wilkie, {Andrew O.M.}",

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TY - JOUR

T1 - Correction

T2 - SMAD6 variants in craniosynostosis: genotype and phenotype evaluation (Genetics in Medicine, (2020), 22, 9, (1498-1506), 10.1038/s41436-020-0817-2)

AU - Genomics England Research Consortium

AU - Calpena, Eduardo

AU - Cuellar, Araceli

AU - Bala, Krithi

AU - Swagemakers, Sigrid M.A.

AU - Koelling, Nils

AU - McGowan, Simon J.

AU - Phipps, Julie M.

AU - Balasubramanian, Meena

AU - Cunningham, Michael L.

AU - Douzgou, Sofia

AU - Lattanzi, Wanda

AU - Morton, Jenny E.V.

AU - Shears, Deborah

AU - Weber, Astrid

AU - Wilson, Louise C.

AU - Lord, Helen

AU - Lester, Tracy

AU - Johnson, David

AU - Wall, Steven A.

AU - Twigg, Stephen R.F.

AU - Mathijssen, Irene M.J.

AU - Boardman-Pretty, Freya

AU - Boyadjiev, Simeon A.

AU - Wilkie, Andrew O.M.

PY - 2020/9/1

Y1 - 2020/9/1

N2 - The version of the Article previously published did not acknowledge Freya Boardman-Pretty17,18 and the Genomics England Research Consortium in the author list. This has now been corrected in both the PDF and HTML versions of the Article. 17Genomics England, London, UK; 18William Harvey Research Institute, Queen Mary University of London, London, UK

AB - The version of the Article previously published did not acknowledge Freya Boardman-Pretty17,18 and the Genomics England Research Consortium in the author list. This has now been corrected in both the PDF and HTML versions of the Article. 17Genomics England, London, UK; 18William Harvey Research Institute, Queen Mary University of London, London, UK

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JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

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