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Journal Abstract Search

169 related items for PubMed ID: 1570839

  • 1.
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  • 2. Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds.
    Gorski SM, Adams KJ, Birch PH, Chodirker BN, Greenberg CR, Goodfellow PJ.
    Hum Genet; 1994 Aug; 94(2):141-8. PubMed ID: 8045560
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  • 4. Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.
    Moore GE, Williamson R, Jensson O, Chambers J, Takakubo F, Newton R, Balacs MA, Ivens A.
    J Craniofac Genet Dev Biol; 1991 Aug; 11(4):372-6. PubMed ID: 1687471
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  • 5. Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.
    Forbes SA, Richardson M, Brennan L, Arnason A, Bjornsson A, Campbell L, Moore G, Stanier P.
    Hum Genet; 1995 Mar; 95(3):342-6. PubMed ID: 7868130
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  • 6. Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region.
    Braybrook C, Warry G, Howell G, Mandryko V, Arnason A, Bjornsson A, Ross MT, Moore GE, Stanier P.
    Hum Genet; 2001 Jun; 108(6):537-45. PubMed ID: 11499681
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  • 7. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P.
    Genomics; 1996 Jan 01; 31(1):36-43. PubMed ID: 8808277
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  • 9. Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.
    Braybrook C, Warry G, Howell G, Arnason A, Bjornsson A, Moore GE, Ross MT, Stanier P.
    Genomics; 2001 Mar 01; 72(2):128-36. PubMed ID: 11401425
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  • 12. Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family.
    Chaabouni M, Smaoui N, Benneji N, M'rad R, Jemaa LB, Hachicha S, Chaabouni H.
    Clin Dysmorphol; 2005 Jan 01; 14(1):23-25. PubMed ID: 15602089
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  • 13. 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 01; 29(2):179-83. PubMed ID: 11559848
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  • 15. Linkage of an X-chromosome cleft palate gene.
    Moore GE, Ivens A, Chambers J, Farrall M, Williamson R, Page DC, Bjornsson A, Arnason A, Jensson O.
    Nature; 2001 Oct 01; 326(6108):91-2. PubMed ID: 2881212
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  • 16. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
    Lesko JG, Lewis RA, Nussbaum RL.
    Am J Hum Genet; 1987 Apr 01; 40(4):303-11. PubMed ID: 2883887
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  • 17. 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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  • 18. Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
    Nussbaum RL, Lewis RA, Lesko JG, Ferrell R.
    Am J Hum Genet; 1985 May 15; 37(3):473-81. PubMed ID: 2988333
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  • 19. A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia.
    Pauws E, Moore GE, Stanier P.
    J Med Genet; 2009 Aug 15; 46(8):555-61. PubMed ID: 19648124
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