يعرض 1 - 20 نتائج من 84 نتيجة بحث عن '"Ashton, G H S"', وقت الاستعلام: 0.99s تنقيح النتائج
  1. 1
    Academic Journal

    المصدر: Fassihi , H , Eady , R A J , Mellerio , J E , Ashton , G H S , Dopping-Hepenstal , P J C , Denyer , J E , Nicolaides , K H , Rodeck , C H & McGrath , J A 2006 , ' Prenatal diagnosis for severe inherited skin disorders: 25 years' experience. ' , British Journal of Dermatology , vol. 154 , no. 1 , pp. 106 - 113 . https://doi.org/10.1111/j.1365-2133.2005.07012.x

  2. 2
    Academic Journal
  3. 3
    Academic Journal

    المصدر: Sethuraman , G , Fassihi , H , Ashton , G H S , Bansal , A , Kabra , M , Sharma , V K & McGrath , J A 2005 , ' An Indian child with Kindler syndrome resulting from a new homozygous non-sense mutation (C468X) in the KIND1 gene. ' , Clinical and Experimental Dermatology , vol. 30 , no. 3 , pp. 286 - 288 . https://doi.org/10.1111/j.1365-2230.2004.01712.x

  4. 4
    Academic Journal

    المصدر: Fassihi , H , Ashton , G H S , Denyer , J E , Mellerio , J E , Mason , G & McGrath , J A 2005 , ' Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in non-idential twins. ' , Clinical and Experimental Dermatology , vol. 30 , no. 2 , pp. 180 - 182 . https://doi.org/10.1111/j.1365-2230.2004.01704.x

  5. 5
    Academic Journal

    المصدر: Fassihi , H , Wessagowit , V , Ashton , G H S , Moss , C , Ward , R , Denyer , J , Mellerio , J E & McGrath , J A 2005 , ' Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa ' , Clinical and Experimental Dermatology , vol. 30 , no. 1 , pp. 71 - 74 . https://doi.org/10.1111/j.1365-2230.2004.01660.x

  6. 6
    Academic Journal

    المصدر: Ashton , G H S , Mclean , W H I & McGrath , J A 2004 , ' Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in kindler syndrome. ' , British Journal of Dermatology , vol. 150 , no. 4 , O3 , pp. 799 - 800 .

  7. 7
    Academic Journal

    المصدر: Thomson , M A , Ashton , G H S , McGrath , J A , Eady , R A J & Moss , C 2004 , ' Retrospective diagnosis of Kindler syndrome in a 37-year-old man ' , BRITISH JOURNAL OF DERMATOLOGY SUPPLEMENT , vol. 151 , P-50 , pp. 43 - 43 .

  8. 8
    Academic Journal

    المصدر: Fassihi , H , Wessagowit , V , Ashton , G H S , Moss , C , Ward , R , Denyer , J , Mellerio , J E & McGrath , J A 2004 , ' Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa ' , BRITISH JOURNAL OF DERMATOLOGY SUPPLEMENT , vol. 151 , PA-8 , pp. 70 - 70 .

  9. 9
    Academic Journal

    المصدر: Fassihi , H , Ashton , G H S , Mellerio , J E , Martinez , A , Atherton , D J , Eady , R A J & McGrath , J A 2004 , ' Improved early diagnosis of Kindler syndrome ' , British Journal of Dermatology , vol. 151 , no. 1 , O13 , pp. 262 - 262 .

  10. 10
    Academic Journal

    المصدر: Fassihi , H , Ashton , G H S , Dopping-Hepenstal , P J C , Denyer , J E , Rodeck , C H , Mellerio , J E , Eady , R A J & McGrath , J A 2004 , ' Twenty-five years' experience of prenatal diagnosis for severe inherited skin disorders ' , BRITISH JOURNAL OF DERMATOLOGY SUPPLEMENT , vol. 151 , RF-2 , pp. 11 - 12 .

  11. 11
    Academic Journal
  12. 12
    Academic Journal
  13. 13
    Academic Journal

    المصدر: Hamada , T , Wessagowit , V , South , A P , Ashton , G H S , Chan , I , Oyama , N , Siriwattana , A , Jewhasuchin , P , Charuwichitratana , S , Thappa , D M , Jeevankumar , B , Lenane , P , Krafchik , B , Kulthanan , K , Shimizu , H , Kaya , T I , Erdal , M E , Paradisi , M , Paller , A S , Seishima , M , Hashimoto , T & McGrath , J A 2003 , ' Extracellular ....

  14. 14
    Academic Journal
  15. 15
    Academic Journal

    المصدر: Fraser-Andrews , E A , Manning , N J , Ashton , G H S , Eldridge , P , McGrath , J & Menage , H D 2003 , ' Fish odour syndrome with features of both primary and secondary trimethylaminuria ' , Clinical and Experimental Dermatology , vol. 28 , no. 2 , pp. 203 - 205 . https://doi.org/10.1046/j.1365-2230.2003.01230.x

  16. 16
    Academic Journal

    المصدر: Ashton , G H S , Smith , F J D , Hamill , K J , White , S J , South , A P , Wessagowit , V , Oyama , N , McLean , W H I & McGrath , J A 2003 , ' Molecular genetics of the actin cytoskeleton disorder Kindler syndrome ' , Journal of Medical Genetics , vol. 40 , pp. S21 - S21 .

  17. 17
    Academic Journal

    المصدر: Millard , T P , Ashton , G H S , Kondeatis , E , Vaughan , R W , Hughes , G R V , Khamashta , M A , Hawk , J L M , McGregor , J M & McGrath , J A 2002 , ' Human Ro60 (SSA2) genomic organization and sequence alterations, examined in cutaneous lupus erythematosus ' , British Journal of Dermatology , vol. 146 , no. 2 , pp. 210 - 215 . https://doi.org/10.1046/j.1365-2133.2002.04618.x

  18. 18
    Academic Journal

    المصدر: Hamada , T , South , A P , Mitsuhashi , Y , Kinebuchi , T , Bleck , O , Ashton , G H S , Hozumi , Y , Suzuki , T , Hashimoto , T , Eady , R A J & McGrath , J A 2002 , ' Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1 ' , Experimental Dermatology , vol. 11 , no. 2 , pp. 107 - 114 . https://doi.org/10.1034/j.1600-0625.2002.110202.x

  19. 19
    Academic Journal
  20. 20
    Academic Journal

    المؤلفون: Ashton, G H S, McGrath, J A, South, A P

    المصدر: Ashton , G H S , McGrath , J A & South , A P 2002 , ' Strategies to identify disease genes ' , DRUGS OF TODAY , vol. 38 , no. 4 , pp. 235 - 244 .