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Journal Abstract Search

144 related items for PubMed ID: 5012690

  • 1. Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
    Gall JC, Stern AM, Poznanski AK, Garn SM, Weinstein ED, Hayward JR.
    Am J Hum Genet; 1972 Jan; 24(1):24-36. PubMed ID: 5012690
    [No Abstract] [Full Text] [Related]

  • 2. Oto-Palato-Digital syndrome with severe X-ray changes in two half brothers.
    Kozlowski K, Turner G, Scougall J, Harrington J.
    Pediatr Radiol; 1977 Sep 01; 6(2):97-102. PubMed ID: 896356
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  • 3. The oto-palato-digital (OPD) syndrome in females.
    Gorlin RJ, Poznanski AK, Hendon I.
    Oral Surg Oral Med Oral Pathol; 1973 Feb 01; 35(2):218-24. PubMed ID: 4513067
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  • 4. [Otopalatodigital syndrome. Apropos of 3 female cases].
    Plenier V, Delaire J, David A, Cohen JY.
    Rev Stomatol Chir Maxillofac; 1983 Feb 01; 84(6):322-9. PubMed ID: 6583818
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  • 5. The oto-palato-digital syndrome. A new symptom-complex consisting of deafness, dwarfism, cleft palate, characteristic facies, and a generalized bone dysplasia.
    Dudding BA, Gorlin RJ, Langer LO.
    Am J Dis Child; 1967 Feb 01; 113(2):214-21. PubMed ID: 6019437
    [No Abstract] [Full Text] [Related]

  • 6. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
    Alembik Y, Stoll C, Messer J.
    Genet Couns; 1997 Feb 01; 8(2):133-7. PubMed ID: 9219012
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  • 7. [A case of dwarfism with oto-palato-digital involvement (author's transl)].
    Farriaux JP, Dubois O, Maroteaux P, Fontaine G.
    J Radiol Electrol Med Nucl; 1974 Feb 01; 55(2):137-42. PubMed ID: 4408413
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  • 10. Inheritance of the oto-palato-digital syndrome.
    Turner G, Gorlin RJ.
    Am J Dis Child; 1970 Apr 01; 119(4):377. PubMed ID: 5434601
    [No Abstract] [Full Text] [Related]

  • 11. Familial bird-headed dwarfism (Seckel's syndrome).
    Sauk JJ, Litt R, Espiritu CE, Delaney JR.
    J Med Genet; 1973 Jun 01; 10(2):196-8. PubMed ID: 4714590
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  • 15. Ruvalcaba syndrome: a case report.
    Bianchi E, Livieri C, Arico M, Cattaneo E, Podesta AF, Beluffi G.
    Eur J Pediatr; 1984 Sep 01; 142(4):301-3. PubMed ID: 6489381
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  • 16. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
    Gurrieri F, Sammito V, Bellussi A, Neri G.
    Am J Med Genet; 1992 Oct 01; 44(3):315-20. PubMed ID: 1488978
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  • 17. An unusual bone dysplasia: parastremmatic dwarfism.
    Langer LO, Petersen D, Spranger J.
    Am J Roentgenol Radium Ther Nucl Med; 1970 Nov 01; 110(3):550-60. PubMed ID: 4992387
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