Gordon CT - Search Results

1

Phenotypic variability of distal 22q11.2 copy number abnormalities.

Tan TY, Collins A, James PA, McGillivray G, Stark Z, Gordon CT, Leventer RJ, Pope K, Forbes R, Crolla JA, Ganesamoorthy D, Burgess T, Bruno DL, Slater HR, Farlie PG, Amor DJ. Tan TY, et al. Among authors: gordon ct. Am J Med Genet A. 2011 Jul;155A(7):1623-33. doi: 10.1002/ajmg.a.34051. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671380

2

The RCAS retroviral expression system in the study of skeletal development.

Gordon CT, Rodda FA, Farlie PG. Gordon CT, et al. Dev Dyn. 2009 Apr;238(4):797-811. doi: 10.1002/dvdy.21907. Dev Dyn. 2009. PMID: 19253393 Free article. Review.

3

Long-range regulation at the SOX9 locus in development and disease.

Gordon CT, Tan TY, Benko S, Fitzpatrick D, Lyonnet S, Farlie PG. Gordon CT, et al. J Med Genet. 2009 Oct;46(10):649-56. doi: 10.1136/jmg.2009.068361. Epub 2009 May 26. J Med Genet. 2009. PMID: 19473998 Review.

4

Developmental perspectives on copy number abnormalities of the 22q11.2 region.

Tan TY, Gordon CT, Amor DJ, Farlie PG. Tan TY, et al. Among authors: gordon ct. Clin Genet. 2010 Sep;78(3):201-18. doi: 10.1111/j.1399-0004.2010.01456.x. Epub 2010 Apr 23. Clin Genet. 2010. PMID: 20497193 Review.

5

Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo.

Gordon CT, Brinas IM, Rodda FA, Bendall AJ, Farlie PG. Gordon CT, et al. Evol Dev. 2010 Sep-Oct;12(5):459-73. doi: 10.1111/j.1525-142X.2010.00432.x. Evol Dev. 2010. PMID: 20883215

6

CXCL14 expression during chick embryonic development.

Gordon CT, Wade C, Brinas I, Farlie PG. Gordon CT, et al. Int J Dev Biol. 2011;55(3):335-40. doi: 10.1387/ijdb.103258cg. Int J Dev Biol. 2011. PMID: 21710440 Free article.

7

Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.

Caruana G, Farlie PG, Hart AH, Bagheri-Fam S, Wallace MJ, Dobbie MS, Gordon CT, Miller KA, Whittle B, Abud HE, Arkell RM, Cole TJ, Harley VR, Smyth IM, Bertram JF. Caruana G, et al. Among authors: gordon ct. PLoS One. 2013;8(3):e55429. doi: 10.1371/journal.pone.0055429. Epub 2013 Mar 1. PLoS One. 2013. PMID: 23469164 Free PMC article.

8

bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1.

Miller KA, Gordon CT, Welfare MF, Caruana G, Bertram JF, Bateman JF, Farlie PG. Miller KA, et al. Among authors: gordon ct. PLoS One. 2013 Oct 15;8(10):e76342. doi: 10.1371/journal.pone.0076342. eCollection 2013. PLoS One. 2013. PMID: 24143185 Free PMC article.

9

YPEL1 overexpression in early avian craniofacial mesenchyme causes mandibular dysmorphogenesis by up-regulating apoptosis.

Tan TY, Gordon CT, Miller KA, Amor DJ, Farlie PG. Tan TY, et al. Among authors: gordon ct. Dev Dyn. 2015 Aug;244(8):1022-30. doi: 10.1002/dvdy.24299. Epub 2015 Jul 16. Dev Dyn. 2015. PMID: 26061551 Free article.

10

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.

Benko S, Fantes JA, Amiel J, Kleinjan DJ, Thomas S, Ramsay J, Jamshidi N, Essafi A, Heaney S, Gordon CT, McBride D, Golzio C, Fisher M, Perry P, Abadie V, Ayuso C, Holder-Espinasse M, Kilpatrick N, Lees MM, Picard A, Temple IK, Thomas P, Vazquez MP, Vekemans M, Roest Crollius H, Hastie ND, Munnich A, Etchevers HC, Pelet A, Farlie PG, Fitzpatrick DR, Lyonnet S. Benko S, et al. Among authors: gordon ct. Nat Genet. 2009 Mar;41(3):359-64. doi: 10.1038/ng.329. Epub 2009 Feb 22. Nat Genet. 2009. PMID: 19234473

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