Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Journal article |
Language: | English |
Published: |
2013
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_version_ | 1797085217465303040 |
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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 | |
first_indexed | 2024-03-07T02:05:49Z |
format | Journal article |
id | oxford-uuid:9ef70f18-b610-418a-9287-740edcc343f2 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T02:05:49Z |
publishDate | 2013 |
record_format | dspace |
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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