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Journal Abstract Search

177 related items for PubMed ID: 11137991

  • 1. Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.
    Mavrogiannis LA, Antonopoulou I, Baxová A, Kutílek S, Kim CA, Sugayama SM, Salamanca A, Wall SA, Morriss-Kay GM, Wilkie AO.
    Nat Genet; 2001 Jan; 27(1):17-8. PubMed ID: 11137991
    [Abstract] [Full Text] [Related]

  • 2. Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
    Mavrogiannis LA, Taylor IB, Davies SJ, Ramos FJ, Olivares JL, Wilkie AO.
    Eur J Hum Genet; 2006 Feb; 14(2):151-8. PubMed ID: 16319823
    [Abstract] [Full Text] [Related]

  • 3. The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).
    Wuyts W, Cleiren E, Homfray T, Rasore-Quartino A, Vanhoenacker F, Van Hul W.
    J Med Genet; 2000 Dec; 37(12):916-20. PubMed ID: 11106354
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  • 4. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2.
    Cohen MM.
    J Craniofac Genet Dev Biol; 2000 Dec; 20(1):19-25. PubMed ID: 10879654
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  • 8. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
    Dobreva G, Chahrour M, Dautzenberg M, Chirivella L, Kanzler B, Fariñas I, Karsenty G, Grosschedl R.
    Cell; 2006 Jun 02; 125(5):971-86. PubMed ID: 16751105
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  • 9. The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly.
    Wöhlke A, Kuiper H, Distl O, Drögemüller C.
    Cytogenet Genome Res; 2006 Jun 02; 115(2):123-8. PubMed ID: 17065792
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  • 10. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.
    Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R.
    Nat Genet; 2000 Apr 02; 24(4):391-5. PubMed ID: 10742104
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  • 11. Clinical and molecular analysis of nine families with Adams-Oliver syndrome.
    Verdyck P, Holder-Espinasse M, Hul WV, Wuyts W.
    Eur J Hum Genet; 2003 Jun 02; 11(6):457-63. PubMed ID: 12774039
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  • 13. Msx homeobox gene family and craniofacial development.
    Alappat S, Zhang ZY, Chen YP.
    Cell Res; 2003 Dec 02; 13(6):429-42. PubMed ID: 14728799
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  • 14. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
    Rujirabanjerd S, Tongsippunyoo K, Sripo T, Limprasert P.
    Eur J Med Genet; 2007 Dec 02; 50(5):346-54. PubMed ID: 17613295
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  • 15. Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.
    Wakui K, Gregato G, Ballif BC, Glotzbach CD, Bailey KA, Kuo PL, Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG.
    Eur J Hum Genet; 2005 May 02; 13(5):528-40. PubMed ID: 15852040
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  • 16. A hole in the head.
    Ferguson MW.
    Nat Genet; 2000 Apr 02; 24(4):330-1. PubMed ID: 10742087
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  • 17. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
    Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, Kocak-Altintas A, Sowden JC, Traboulsi E, Sarfarazi M, McInnes RR.
    Nat Genet; 2000 Aug 02; 25(4):397-401. PubMed ID: 10932181
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  • 18. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
    Köchling J, Karbasiyan M, Reis A.
    Eur J Hum Genet; 2001 Aug 02; 9(8):599-605. PubMed ID: 11528505
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  • 19. Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration.
    Liu W, Selever J, Lu MF, Martin JF.
    Development; 2003 Dec 02; 130(25):6375-85. PubMed ID: 14623826
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  • 20. A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.
    Stegmann K, Boecker J, Richter B, Capra V, Finnell RH, Ngo ET, Strehl E, Ermert A, Koch MC.
    Teratology; 2001 May 02; 63(5):167-75. PubMed ID: 11320527
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