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Journal Abstract Search

226 related items for PubMed ID: 8981943

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  • 2. Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
    Unden AB, Holmberg E, Lundh-Rozell B, Stähle-Bäckdahl M, Zaphiropoulos PG, Toftgård R, Vorechovsky I.
    Cancer Res; 1996 Oct 15; 56(20):4562-5. PubMed ID: 8840960
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  • 9. De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.
    Wicking C, Gillies S, Smyth I, Shanley S, Fowles L, Ratcliffe J, Wainwright B, Chenevix-Trench G.
    Am J Med Genet; 1997 Dec 19; 73(3):304-7. PubMed ID: 9415689
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  • 15. Nevoid basal cell carcinoma syndrome - clinical manifestations and mutation analysis of a Taiwanese family.
    Chung CH, Wong TY, Shieh TY, Shieh DB, Chao SC.
    J Formos Med Assoc; 2003 Nov 19; 102(11):793-7. PubMed ID: 14724726
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  • 16. PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients.
    Li TJ, Yuan JW, Gu XM, Sun LS, Zhao HS.
    Oral Dis; 2008 Mar 19; 14(2):174-9. PubMed ID: 18302678
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  • 17. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes.
    Richards FM, Goudie DR, Cooper WN, Jene Q, Barroso I, Wicking C, Wainwright BJ, Ferguson-Smith MA.
    Hum Genet; 1997 Dec 19; 101(3):317-22. PubMed ID: 9439661
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  • 18. Analysis of mutation in exon 17 of PTCH in patients with nevoid basal cell carcinoma syndrome.
    Li J, Wang J, Liu Y, Wang W.
    Mol Biol Rep; 2010 Jan 19; 37(1):359-62. PubMed ID: 19728145
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