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Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.
Dev Dyn. 2014 Sep;243(9):1143-51. doi: 10.1002/dvdy.24147. Epub 2014 Jun 12.
Dev Dyn. 2014.
PMID: 24812002
Free PMC article.
Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.
Whittaker DE, Kasah S, Donovan APA, Ellegood J, Riegman KLH, Volk HA, McGonnell I, Lerch JP, Basson MA.
Whittaker DE, et al. Among authors: kasah s.
Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):n/a. doi: 10.1002/ajmg.c.31595. Epub 2017 Nov 23.
Am J Med Genet C Semin Med Genet. 2017.
PMID: 29168327
Free PMC article.
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Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes.
Kasah S, Oddy C, Basson MA.
Kasah S, et al.
J Anat. 2018 Dec;233(6):755-769. doi: 10.1111/joa.12889. Epub 2018 Oct 2.
J Anat. 2018.
PMID: 30277262
Free PMC article.
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The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression.
Whittaker DE, Riegman KL, Kasah S, Mohan C, Yu T, Pijuan-Sala B, Hebaishi H, Caruso A, Marques AC, Michetti C, Smachetti ME, Shah A, Sabbioni M, Kulhanci O, Tee WW, Reinberg D, Scattoni ML, Volk H, McGonnell I, Wardle FC, Fernandes C, Basson MA.
Whittaker DE, et al. Among authors: kasah s.
J Clin Invest. 2017 Mar 1;127(3):874-887. doi: 10.1172/JCI83408. Epub 2017 Feb 6.
J Clin Invest. 2017.
PMID: 28165338
Free PMC article.
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