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Journal Abstract Search

118 related items for PubMed ID: 14729838

  • 1. TBX22 mutations are a frequent cause of cleft palate.
    Marçano AC, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P.
    J Med Genet; 2004 Jan; 41(1):68-74. PubMed ID: 14729838
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  • 2. Novel TBX22 mutations in Chinese nonsyndromic cleft lip/palate families.
    Dai J, Xu C, Wang G, Liang Y, Wan T, Zhang Y, Xu X, Yu L, Che Z, Han Q, Wu D, Yang Y.
    J Genet; 2018 Jun; 97(2):411-417. PubMed ID: 29932061
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  • 3. TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.
    Andreou AM, Pauws E, Jones MC, Singh MK, Bussen M, Doudney K, Moore GE, Kispert A, Brosens JJ, Stanier P.
    Am J Hum Genet; 2007 Oct; 81(4):700-12. PubMed ID: 17846996
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  • 7. Cloning and expression analysis of the chick ortholog of TBX22, the gene mutated in X-linked cleft palate and ankyloglossia.
    Haenig B, Schmidt C, Kraus F, Pfordt M, Kispert A.
    Mech Dev; 2002 Sep; 117(1-2):321-5. PubMed ID: 12204278
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  • 9. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
    Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P.
    Nat Genet; 2001 Oct; 29(2):179-83. PubMed ID: 11559848
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  • 10. Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.
    Braybrook C, Lisgo S, Doudney K, Henderson D, Marçano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S.
    Hum Mol Genet; 2002 Oct 15; 11(22):2793-804. PubMed ID: 12374769
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  • 11. Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
    Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P.
    J Dent Res; 2011 Apr 15; 90(4):450-5. PubMed ID: 21248356
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  • 17. Wieacker-Wolff syndrome with associated cleft palate in a female case.
    Godfrey ND, Dowlatshahi S, Martin MM, Rothkopf DM.
    Am J Med Genet A; 2018 Jan 15; 176(1):167-170. PubMed ID: 29150902
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  • 19. Time for T.
    Murray JC.
    Nat Genet; 2001 Oct 15; 29(2):107-9. PubMed ID: 11586288
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  • 20. Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate.
    Koivisto AM, Ala-Mello S, Lemmelä S, Komu HA, Rautio J, Järvelä I.
    Clin Genet; 2007 Aug 15; 72(2):145-9. PubMed ID: 17661819
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