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Journal Abstract Search

189 related items for PubMed ID: 1605259

  • 1. Apparent cleidocranial dysplasia associated with abnormalities of 8q22 in three individuals.
    Brueton LA, Reeve A, Ellis R, Husband P, Thompson EM, Kingston HM.
    Am J Med Genet; 1992 Jun 01; 43(3):612-8. PubMed ID: 1605259
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  • 2. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.
    Visosky AM, Johnson J, Bingea B, Gurney T, Lalwani AK.
    Laryngoscope; 2003 Sep 01; 113(9):1508-14. PubMed ID: 12972925
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  • 3. Syndromes and situations associated with congenital clavicular hypoplasia or agenesis.
    Hall BD.
    Prog Clin Biol Res; 1982 Sep 01; 104():279-88. PubMed ID: 7163272
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  • 7. A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.
    Feldman GJ, Robin NH, Brueton LA, Robertson E, Thompson EM, Siegel-Bartelt J, Gasser DL, Bailey LC, Zackai EH, Muenke M.
    Am J Hum Genet; 1995 Apr 01; 56(4):938-43. PubMed ID: 7717404
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  • 9. Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion.
    Gelb BD, Cooper E, Shevell M, Desnick RJ.
    Am J Med Genet; 1995 Aug 28; 58(2):200-5. PubMed ID: 8533817
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  • 10. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression].
    Stoll C, Roth MP, Hessemann H, Paira M.
    Arch Fr Pediatr; 1983 Dec 28; 40(10):763-6. PubMed ID: 6673680
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  • 11. [Pierre Marie-Sainton cleidocranial dysplasia].
    Diaconescu S, Păduraru G, Vâscu AM, Burlea M.
    Rev Med Chir Soc Med Nat Iasi; 2011 Dec 28; 115(2):341-8. PubMed ID: 21870721
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  • 12. [Orthodontic and oral surgery therapy in cleidocranial dysplasia].
    Balaton G, Tarján I, Balaton P, Barabási Z, Gyulai Gál S, Nagy K, Vajó Z.
    Fogorv Sz; 2007 Feb 28; 100(1):17-21. PubMed ID: 17444132
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  • 14. Intrafamilial variability in cleidocranial dysplasia: a three generation family.
    Chitayat D, Hodgkinson KA, Azouz EM.
    Am J Med Genet; 1992 Feb 01; 42(3):298-303. PubMed ID: 1536165
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  • 15. Malformation syndromes in human genetic disease.
    Nyhan WL.
    Plast Reconstr Surg; 1973 Sep 01; 52(3):237-45. PubMed ID: 4269199
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  • 17. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.
    Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K.
    Orthod Craniofac Res; 2007 Nov 01; 10(4):222-5. PubMed ID: 17973689
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  • 18. [Cleidocranial dysplasia: a case report].
    Kanda M, Kabe S, Kanki T, Sato J, Hasegawa Y.
    No Shinkei Geka; 1997 Dec 01; 25(12):1109-13. PubMed ID: 9430147
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  • 19. A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
    Northup JK, Matalon R, Lockhart LH, Hawkins JC, Velagaleti GV.
    Eur J Med Genet; 2011 Dec 01; 54(4):e394-8. PubMed ID: 21466863
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  • 20. Pericentric inversion of chromosome 6 in a patient with cleidocranial dysplasia.
    Nienhaus H, Mau U, Zang KD, Henn W.
    Am J Med Genet; 1993 Jul 01; 46(6):630-1. PubMed ID: 8362902
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