Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

VP Sharma; AL Fenwick; MS Brockop; SJ McGowan; Jacqueline Goos; Jeannette Hoogeboom; AF Brady; NO Jeelani; SA Lynch; JB Mulliken; DJ Murray; JM Phipps; E Sweeney; SE Tomkins; LC Wilson; S Bennett; RJ Cornall; J Broxholme; A Kanapin; D Johnson; SA Wall; Peter van der Spek; Irene Mathijssen; RE Maxson; SRF Twigg; AOM Wilkie

doi:10.1038/ng.2531

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

VP Sharma, AL Fenwick, MS Brockop, SJ McGowan, Jacqueline Goos, Jeannette Hoogeboom, AF Brady, NO Jeelani, SA Lynch, JB Mulliken, DJ Murray, JM Phipps, E Sweeney, SE Tomkins, LC Wilson, S Bennett, RJ Cornall, J Broxholme, A Kanapin, D JohnsonSA Wall, Peter van der Spek, Irene Mathijssen, RE Maxson, SRF Twigg, AOM Wilkie

Research output: Contribution to journal › Article › Academic › peer-review

191 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	304-307
Number of pages	4
Journal	Nature Genetics
Volume	45
Issue number	3
DOIs	https://doi.org/10.1038/ng.2531
Publication status	Published - 2013

Research programs

EMC MGC-02-02-01
EMC MGC-02-96-01
EMC NIHES-01-50-01-A

Access to Document

10.1038/ng.2531

http://hdl.handle.net/1765/40850

Cite this

Sharma, VP., Fenwick, AL., Brockop, MS., McGowan, SJ., Goos, J., Hoogeboom, J., Brady, AF., Jeelani, NO., Lynch, SA., Mulliken, JB., Murray, DJ., Phipps, JM., Sweeney, E., Tomkins, SE., Wilson, LC., Bennett, S., Cornall, RJ., Broxholme, J., Kanapin, A., ... Wilkie, AOM. (2013). Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Nature Genetics, 45(3), 304-307. https://doi.org/10.1038/ng.2531

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author = "VP Sharma and AL Fenwick and MS Brockop and SJ McGowan and Jacqueline Goos and Jeannette Hoogeboom and AF Brady and NO Jeelani and SA Lynch and JB Mulliken and DJ Murray and JM Phipps and E Sweeney and SE Tomkins and LC Wilson and S Bennett and RJ Cornall and J Broxholme and A Kanapin and D Johnson and SA Wall and {van der Spek}, Peter and Irene Mathijssen and RE Maxson and SRF Twigg and AOM Wilkie",

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Sharma, VP, Fenwick, AL, Brockop, MS, McGowan, SJ, Goos, J, Hoogeboom, J, Brady, AF, Jeelani, NO, Lynch, SA, Mulliken, JB, Murray, DJ, Phipps, JM, Sweeney, E, Tomkins, SE, Wilson, LC, Bennett, S, Cornall, RJ, Broxholme, J, Kanapin, A, Johnson, D, Wall, SA, van der Spek, P , Mathijssen, I, Maxson, RE, Twigg, SRF & Wilkie, AOM 2013, 'Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis', Nature Genetics, vol. 45, no. 3, pp. 304-307. https://doi.org/10.1038/ng.2531

TY - JOUR

T1 - Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

AU - Sharma, VP

AU - Fenwick, AL

AU - Brockop, MS

AU - McGowan, SJ

AU - Goos, Jacqueline

AU - Hoogeboom, Jeannette

AU - Brady, AF

AU - Jeelani, NO

AU - Lynch, SA

AU - Mulliken, JB

AU - Murray, DJ

AU - Phipps, JM

AU - Sweeney, E

AU - Tomkins, SE

AU - Wilson, LC

AU - Bennett, S

AU - Cornall, RJ

AU - Broxholme, J

AU - Kanapin, A

AU - Johnson, D

AU - Wall, SA

AU - van der Spek, Peter

AU - Mathijssen, Irene

AU - Maxson, RE

AU - Twigg, SRF

AU - Wilkie, AOM

PY - 2013

Y1 - 2013

U2 - 10.1038/ng.2531

DO - 10.1038/ng.2531

M3 - Article

C2 - 23354436

SN - 1061-4036

VL - 45

SP - 304

EP - 307

JO - Nature Genetics

JF - Nature Genetics

IS - 3

ER -