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Journal Abstract Search

349 related items for PubMed ID: 8696335

  • 1. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
    Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
    Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
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  • 2. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
    Mostowska A, Biedziak B, Jagodzinski PP.
    Arch Oral Biol; 2012 Jun; 57(6):790-5. PubMed ID: 22297032
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  • 3. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2.
    Cohen MM.
    J Craniofac Genet Dev Biol; 2000 Jun; 20(1):19-25. PubMed ID: 10879654
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  • 4. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.
    Goldenberg M, Das P, Messersmith M, Stockton DW, Patel PI, D'Souza RN.
    J Dent Res; 2000 Jul; 79(7):1469-75. PubMed ID: 11005730
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  • 5. The role of MSX1 in human tooth agenesis.
    Lidral AC, Reising BC.
    J Dent Res; 2002 Apr; 81(4):274-8. PubMed ID: 12097313
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  • 11. A nonsense mutation in MSX1 causes Witkop syndrome.
    Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR.
    Am J Hum Genet; 2001 Jul; 69(1):67-74. PubMed ID: 11369996
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  • 14. Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.
    Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I.
    Hum Genet; 1995 Sep; 96(3):305-8. PubMed ID: 7649547
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  • 15. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
    Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H.
    Eur J Oral Sci; 2007 Aug; 115(4):330-3. PubMed ID: 17697174
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  • 16. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
    Ma X, Li FF, Wang SZ, Gao C, Zhang M, Zhu SQ.
    Mol Vis; 2008 Aug; 14():1906-11. PubMed ID: 18958306
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  • 17. Studies on Pax9-Msx1 protein interactions.
    Ogawa T, Kapadia H, Wang B, D'Souza RN.
    Arch Oral Biol; 2005 Feb; 50(2):141-5. PubMed ID: 15721141
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  • 18. Molecular morphogenetic fields in the development of human dentition.
    Line SR.
    J Theor Biol; 2001 Jul 07; 211(1):67-75. PubMed ID: 11407892
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