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

Bibliographic Details
Main Authors: Sharma, V, Fenwick, A, Brockop, MS, McGowan, S, Goos, J, Hoogeboom, A, Brady, A, Jeelani, N, Lynch, SA, Mulliken, J, Murray, D, Phipps, J, Sweeney, E, Tomkins, SE, Wilson, L, Bennett, S, Cornall, R, Broxholme, J, Kanapin, A, 500 Whole-Genome Sequences (WGS500) Consortium, Johnson, D, Wall, SA, van der Spek, P, Mathijssen, I, Maxson, R
Format: Journal article
Language:English
Published: 2013
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author Sharma, V
Fenwick, A
Brockop, MS
McGowan, S
Goos, J
Hoogeboom, A
Brady, A
Jeelani, N
Lynch, SA
Mulliken, J
Murray, D
Phipps, J
Sweeney, E
Tomkins, SE
Wilson, L
Bennett, S
Cornall, R
Broxholme, J
Kanapin, A
500 Whole-Genome Sequences (WGS500) Consortium
Johnson, D
Wall, SA
van der Spek, P
Mathijssen, I
Maxson, R
author_facet Sharma, V
Fenwick, A
Brockop, MS
McGowan, S
Goos, J
Hoogeboom, A
Brady, A
Jeelani, N
Lynch, SA
Mulliken, J
Murray, D
Phipps, J
Sweeney, E
Tomkins, SE
Wilson, L
Bennett, S
Cornall, R
Broxholme, J
Kanapin, A
500 Whole-Genome Sequences (WGS500) Consortium
Johnson, D
Wall, SA
van der Spek, P
Mathijssen, I
Maxson, R
author_sort Sharma, V
collection OXFORD
description
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id oxford-uuid:9ef70f18-b610-418a-9287-740edcc343f2
institution University of Oxford
language English
last_indexed 2024-03-07T02:05:49Z
publishDate 2013
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spelling oxford-uuid:9ef70f18-b610-418a-9287-740edcc343f22022-03-27T00:54:00ZMutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9ef70f18-b610-418a-9287-740edcc343f2EnglishSymplectic Elements at Oxford2013Sharma, VFenwick, ABrockop, MSMcGowan, SGoos, JHoogeboom, ABrady, AJeelani, NLynch, SAMulliken, JMurray, DPhipps, JSweeney, ETomkins, SEWilson, LBennett, SCornall, RBroxholme, JKanapin, A500 Whole-Genome Sequences (WGS500) ConsortiumJohnson, DWall, SAvan der Spek, PMathijssen, IMaxson, R
spellingShingle Sharma, V
Fenwick, A
Brockop, MS
McGowan, S
Goos, J
Hoogeboom, A
Brady, A
Jeelani, N
Lynch, SA
Mulliken, J
Murray, D
Phipps, J
Sweeney, E
Tomkins, SE
Wilson, L
Bennett, S
Cornall, R
Broxholme, J
Kanapin, A
500 Whole-Genome Sequences (WGS500) Consortium
Johnson, D
Wall, SA
van der Spek, P
Mathijssen, I
Maxson, R
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title_full Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title_fullStr Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title_full_unstemmed Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title_short Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
title_sort mutations in tcf12 encoding a basic helix loop helix partner of twist1 are a frequent cause of coronal craniosynostosis
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