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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

158 related items for PubMed ID: 25869409

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  • 3. GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families.
    Patel R, Singh CB, Bhattacharya V, Singh SK, Ali A.
    Congenit Anom (Kyoto); 2016 Mar; 56(2):94-7. PubMed ID: 26508445
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  • 6. A novel frameshift mutation of the GLI3 gene in a family with broad thumbs with/without big toes, postaxial polydactyly and variable syndactyly of the hands/feet.
    Al-Qattan MM.
    Clin Genet; 2012 Nov; 82(5):502-4. PubMed ID: 22428873
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  • 7. A novel missense in GLI3 possibly affecting one of the zinc finger domains may lead to postaxial synpolydactyly: case report.
    Zou Q, Tian Z, Zheng J, Zhi X, Du X, Shu J, Cai C.
    BMC Med Genet; 2019 Nov 09; 20(1):174. PubMed ID: 31706290
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  • 8. Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.
    Tanteles GA, Michaelidou S, Loukianou E, Christophidou-Anastasiadou V, Kleopa KA.
    Clin Dysmorphol; 2015 Jul 09; 24(3):102-5. PubMed ID: 25714367
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  • 9. A novel frame-shift mutation of GLI3 causes non-syndromic and complex digital anomalies in a Chinese family.
    Cheng F, Ke X, Lv M, Zhang F, Li C, Zhang X, Zhang Y, Zhao X, Wang X, Liu B, Han J, Li Y, Zeng C, Li S.
    Clin Chim Acta; 2011 May 12; 412(11-12):1012-7. PubMed ID: 21320477
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  • 11. A Novel Frameshift Mutation of GLI3 Causes Isolated Postaxial Polydactyly.
    Ni F, Han G, Guo R, Cui H, Wang B, Li Q.
    Ann Plast Surg; 2019 May 12; 82(5):570-573. PubMed ID: 30562203
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  • 12. GLI2 mutations typically result in pituitary anomalies with or without postaxial polydactyly.
    Bear KA, Solomon BD.
    Am J Med Genet A; 2015 Oct 12; 167A(10):2491-2. PubMed ID: 25974718
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  • 13. The pathogenesis of ulnar polydactyly in humans.
    Al-Qattan MM, Al-Motairi MI.
    J Hand Surg Eur Vol; 2013 Nov 12; 38(9):934-9. PubMed ID: 23435486
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  • 14. 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 Nov 12; 19(3):228-235. PubMed ID: 30848202
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  • 15. Two Indian families with Greig cephalopolysyndactyly with non-syndromic phenotype.
    Sethi SK, Goyal D, Khalil S, Yadav DK.
    Eur J Pediatr; 2013 Aug 12; 172(8):1131-5. PubMed ID: 23334564
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  • 16. Advances in the molecular genetics of non-syndromic polydactyly.
    Deng H, Tan T, Yuan L.
    Expert Rev Mol Med; 2015 Oct 30; 17():e18. PubMed ID: 26515020
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  • 17. A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex.
    Volodarsky M, Langer Y, Birk OS.
    BMC Med Genet; 2014 Sep 30; 15():110. PubMed ID: 25267529
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  • 18. A novel variant of GLI3, p.Asp1514Thrfs*5, is identified in a Chinese family affected by polydactyly.
    Wang Y, Hao X, Jia X, Ji W, Yuan S, Gnamey EJA, Huang M, Xu L, Zhang X, Bai J, Sun W, Fu S, Liu Y, Wu J.
    Mol Genet Genomic Med; 2022 Jul 30; 10(7):e1968. PubMed ID: 35546307
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  • 19. A novel missense variant in the GLI3 zinc finger domain in a family with digital anomalies.
    Crapster JA, Hudgins L, Chen JK, Gomez-Ospina N.
    Am J Med Genet A; 2017 Dec 30; 173(12):3221-3225. PubMed ID: 28884880
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  • 20. A GLI3 variant leading to polydactyly in heterozygotes and Pallister-Hall-like syndrome in a homozygote.
    Kariminejad A, Ghaderi-Sohi S, Keshavarz E, Hashemi SA, Parsimehr E, Szenker-Ravi E, Khatoo M, Faraji Zonooz M, Reversade B, Najmabadi H, Hennekam RC.
    Clin Genet; 2020 Jun 30; 97(6):915-919. PubMed ID: 32112393
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