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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2013 | 1 |
2015 | 1 |
2017 | 1 |
2018 | 1 |
2019 | 1 |
2024 | 0 |
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Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.
Nat Genet. 2013 Mar;45(3):308-13. doi: 10.1038/ng.2539. Epub 2013 Jan 27.
Nat Genet. 2013.
PMID: 23354439
Free PMC article.
Heterozygous mutations in ERF cause syndromic craniosynostosis with multiple suture involvement.
Chaudhry A, Sabatini P, Han L, Ray PN, Forrest C, Bowdin S.
Chaudhry A, et al.
Am J Med Genet A. 2015 Nov;167A(11):2544-7. doi: 10.1002/ajmg.a.37218. Epub 2015 Jun 22.
Am J Med Genet A. 2015.
PMID: 26097063
Item in Clipboard
A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations.
Lee E, Le T, Zhu Y, Elakis G, Turner A, Lo W, Venselaar H, Verrenkamp CA, Snow N, Mowat D, Kirk EP, Sachdev R, Smith J, Brown NJ, Wallis M, Barnett C, McKenzie F, Freckmann ML, Collins F, Chopra M, Gregersen N, Hayes I, Rajagopalan S, Tan TY, Stark Z, Savarirayan R, Yeung A, Adès L, Gattas M, Gibson K, Gabbett M, Amor DJ, Lattanzi W, Boyd S, Haan E, Gianoutsos M, Cox TC, Buckley MF, Roscioli T.
Lee E, et al.
Genet Med. 2018 Sep;20(9):1061-1068. doi: 10.1038/gim.2017.214. Epub 2017 Dec 7.
Genet Med. 2018.
PMID: 29215649
Free article.
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ERF-related craniosynostosis: The phenotypic and developmental profile of a new craniosynostosis syndrome.
Glass GE, O'Hara J, Canham N, Cilliers D, Dunaway D, Fenwick AL, Jeelani NO, Johnson D, Lester T, Lord H, Morton JEV, Nishikawa H, Noons P, Schwiebert K, Shipster C, Taylor-Beadling A, Twigg SRF, Vasudevan P, Wall SA, Wilkie AOM, Wilson LC.
Glass GE, et al.
Am J Med Genet A. 2019 Apr;179(4):615-627. doi: 10.1002/ajmg.a.61073. Epub 2019 Feb 13.
Am J Med Genet A. 2019.
PMID: 30758909
Free PMC article.
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