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| 1 | EEC (Ectrodactyly,Ectodermal dysplasia,Clefting) syndrome:heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis显示文摘 | South AP Ashton GH Willoughby C Ellis IH Bleck O Hamada T | 2002 | Br J Dermatol2002，146，2： | 1 |
| 2 | EEC (Ectro- dactyly, Ectodermal dysplasia, Clefting) syndrome: Hetero- zygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis显示文摘 | South AP Ashton GH Willoughby C | 2002 | Br J Dermatol2002，146，2： | 1 |
| 3 | Focal adhesion kinase is required for intestinal regeneration and tumorigenesis downstream of Wnt/c-Myc signaling显示文摘 | Ashton GH Morton JP Myant K | 2010 | Developmental Cell2010，19，2： | 1 |
| 4 | Loss of kindlin-1,a human homolog of the Caenorhabditis elegans actin-extracellularmatrix linker protein UNC-112,causes Kindler syndrome显示文摘 | Siegel DH Ashton GH Penagos HG | 2003 | Am J Hum Genet2003，73，1： | 1 |
| 5 | Kindler syndrome显示文摘 | Ashton GH | 2004 | Clin Exp Dermatol2004，29，2： | 1 |
| 6 | Kindler syndrome显示文摘 | Ashton GH | 2004 | Clin Exp Dermatol2004，29，2： | 1 |
| 7 | Recurrent mutations in kindlin-1,a novel keratinocyte focal contact protein,in the autosoreal recessive skin fragility and photosensitivity disorder,Kindler syndrome显示文摘 | Ashton GH McLean WH South AP | 2004 | J Invest Dermatol2004，122，1： | 1 |
| 8 | Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actinextracellular-matrix linker protein UNC-112, causes Kindler syndrome 显示文摘 | Siegel DH Ashton GH Penagos HG | 2003 | Am J Hum Genet2003，73，： | 1 |
| 9 | Alpha 6 beta 4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresia 显示文摘 | Ashton GH Sorelli P Mellerio J | 2001 | Br J Demmtol2001，144，： | 1 |
| 10 | Striate Palmoplantar Keratodcrma resulting from desmoplakin haploinsufficicney显示文摘 | Whittock NV Ashton GH Dopping-Hepenstal PJ | 1999 | J Invest Dcrmatol1999，113，6： | 1 |
| 11 | Loss of kindlin-1,a human homolog of the Caenorhabditis elegans actin-extracellular matrix linker protein UNC-112,causes Kindler syndrome显示文摘 | Siegel DH Ashton GH Penagos HG | | 0，，01： | 1 |
| 12 | New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroder- ma and keratin 2e that cause ichthyosis bullosa of Siemens 显示文摘 | Whittock NV Ashton GH Griffiths WA | 2001 | Br J Dermatol2001，145，2： | 1 |
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