Stanier P - Search Results

1

Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region.

Braybrook C, Warry G, Howell G, Mandryko V, Arnason A, Bjornsson A, Ross MT, Moore GE, Stanier P. Braybrook C, et al. Among authors: stanier p. Hum Genet. 2001 Jun;108(6):537-45. doi: 10.1007/s004390100518. Hum Genet. 2001. PMID: 11499681

2

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

Braybrook C, Lisgo S, Doudney K, Henderson D, Marçano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S. Braybrook C, et al. Among authors: stanier p. Hum Mol Genet. 2002 Oct 15;11(22):2793-804. doi: 10.1093/hmg/11.22.2793. Hum Mol Genet. 2002. PMID: 12374769

3

Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.

Stanier P, Moore GE. Stanier P, et al. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R73-81. doi: 10.1093/hmg/ddh052. Epub 2004 Jan 13. Hum Mol Genet. 2004. PMID: 14722155 Review.

4

Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.

Forbes SA, Richardson M, Brennan L, Arnason A, Bjornsson A, Campbell L, Moore G, Stanier P. Forbes SA, et al. Among authors: stanier p. Hum Genet. 1995 Mar;95(3):342-6. doi: 10.1007/BF00225205. Hum Genet. 1995. PMID: 7868130

5

Novel RFLPs and microsatellite repeats increase informativity at four loci mapping to Xq22-q25.

Newton R, Stanier P, Forbes S, Moore GE. Newton R, et al. Among authors: stanier p. Hum Genet. 1994 Feb;93(2):218-21. doi: 10.1007/BF00210618. Hum Genet. 1994. PMID: 7906669

6

The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.

Stanier P, Forbes SA, Arnason A, Bjornsson A, Sveinbjornsdottir E, Williamson R, Moore G. Stanier P, et al. Genomics. 1993 Sep;17(3):549-55. doi: 10.1006/geno.1993.1370. Genomics. 1993. PMID: 8244369

7

Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.

Braybrook C, Warry G, Howell G, Arnason A, Bjornsson A, Moore GE, Ross MT, Stanier P. Braybrook C, et al. Among authors: stanier p. Genomics. 2001 Mar 1;72(2):128-36. doi: 10.1006/geno.2000.6478. Genomics. 2001. PMID: 11401425

8

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P. Braybrook C, et al. Among authors: stanier p. Nat Genet. 2001 Oct;29(2):179-83. doi: 10.1038/ng730. Nat Genet. 2001. PMID: 11559848

9

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. Monk D, et al. Among authors: stanier p. Hum Genet. 2002 Oct;111(4-5):376-87. doi: 10.1007/s00439-002-0777-4. Epub 2002 Aug 16. Hum Genet. 2002. PMID: 12384779

10

Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.

Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F. Zhou H, et al. Among authors: stanier p. Am J Hum Genet. 2006 Nov;79(5):859-68. doi: 10.1086/508500. Epub 2006 Sep 21. Am J Hum Genet. 2006. PMID: 17033962 Free PMC article.

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