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Journal Abstract Search

417 related items for PubMed ID: 7702086

  • 1. A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia.
    Stoilov I, Kilpatrick MW, Tsipouras P.
    Am J Med Genet; 1995 Jan 02; 55(1):127-33. PubMed ID: 7702086
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  • 2. [Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
    Ezquieta Zubicaray B, Iguacel AO, Varela Junquera JM, Jariego Fente CM, González Gancedo P, Gracia Bouthelier R.
    Med Clin (Barc); 1999 Mar 06; 112(8):290-3. PubMed ID: 10207844
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  • 3. [Mutations in the Fibroblast Growth Factor Receptor 3 gene (FGFR3) in Chilean patients with idiopathic short stature, hypochondroplasia and achondroplasia].
    Mancilla EE, Poggi H, Repetto G, García C, Foradori A, Cattani A.
    Rev Med Chil; 2003 Dec 06; 131(12):1405-10. PubMed ID: 15022403
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  • 5. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
    Rousseau F, Bonaventure J, Legeai-Mallet L, Pelet A, Rozet JM, Maroteaux P, Le Merrer M, Munnich A.
    Nature; 1994 Sep 15; 371(6494):252-4. PubMed ID: 8078586
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  • 6. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.
    Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, Greenhaw GA, Hecht JT, Francomano CA.
    Nat Genet; 1995 Jul 15; 10(3):357-9. PubMed ID: 7670477
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  • 7. A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. Online.
    Grigelioniené G, Hagenäs L, Eklöf O, Neumeyer L, Haereid PE, Anvret M.
    Hum Mutat; 1998 Jul 15; 11(4):333. PubMed ID: 10215410
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  • 13. Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene.
    Pehlivan S, Ozkinay F, Okutman O, Coğulu O, Ozcan A, Cankaya T, Ulgenalp A.
    Turk J Pediatr; 2003 Jul 15; 45(2):99-101. PubMed ID: 12921294
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  • 14. Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data.
    Tsai FJ, Tsai CH, Chang JG, Wu JY.
    Am J Med Genet; 1999 Sep 17; 86(3):300-1. PubMed ID: 10482885
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  • 18. [Mutation analysis of fibroblast growth factor receptor 3 gene in an achondroplasia family].
    Zhu B, Dong QM, Huang XH, Ji GQ, Chen Y, Wang WX, Jiang HY, Gao JS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct 17; 20(5):373-5. PubMed ID: 14556186
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  • 20. A common FGFR3 gene mutation in hypochondroplasia.
    Prinos P, Costa T, Sommer A, Kilpatrick MW, Tsipouras P.
    Hum Mol Genet; 1995 Nov 17; 4(11):2097-101. PubMed ID: 8589686
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