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PUBMED FOR HANDHELDS

Journal Abstract Search


240 related items for PubMed ID: 26508445

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  • 2. Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients.
    Wang Z, Wang J, Li Y, Geng J, Fu Q, Xu Y, Shen Y.
    Clin Chim Acta; 2014 Jun 10; 433():195-9. PubMed ID: 24667698
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  • 15. Letter to the editor regarding: "Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients" Clinica Chimica acta 433 (2014) 195-199.
    Baas M, Galjaard RJ, der Spek Pv, Hovius SE, van Nieuwenhoven CA.
    Clin Chim Acta; 2015 Jul 20; 447():71. PubMed ID: 25869409
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  • 16. Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation.
    Mumtaz S, Yıldız E, Lal K, Tolun A, Malik S.
    Eur J Med Genet; 2017 May 20; 60(5):268-274. PubMed ID: 28315472
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  • 17. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
    Kang S, Graham JM, Olney AH, Biesecker LG.
    Nat Genet; 1997 Mar 20; 15(3):266-8. PubMed ID: 9054938
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  • 18. Novel GLI3 Mutations in Chinese Patients with Non-syndromic Post-axial Polydactyly.
    Chen X, Yuan L, Xu H, Hu P, Yang Y, Guo Y, Guo Z, Deng H.
    Curr Mol Med; 2019 Mar 20; 19(3):228-235. PubMed ID: 30848202
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  • 20. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
    Johnston JJ, Olivos-Glander I, Killoran C, Elson E, Turner JT, Peters KF, Abbott MH, Aughton DJ, Aylsworth AS, Bamshad MJ, Booth C, Curry CJ, David A, Dinulos MB, Flannery DB, Fox MA, Graham JM, Grange DK, Guttmacher AE, Hannibal MC, Henn W, Hennekam RC, Holmes LB, Hoyme HE, Leppig KA, Lin AE, Macleod P, Manchester DK, Marcelis C, Mazzanti L, McCann E, McDonald MT, Mendelsohn NJ, Moeschler JB, Moghaddam B, Neri G, Newbury-Ecob R, Pagon RA, Phillips JA, Sadler LS, Stoler JM, Tilstra D, Walsh Vockley CM, Zackai EH, Zadeh TM, Brueton L, Black GC, Biesecker LG.
    Am J Hum Genet; 2005 Apr 20; 76(4):609-22. PubMed ID: 15739154
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