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Journal Abstract Search

134 related items for PubMed ID: 5727172

  • 1. [Chromosomal study in otosclerosis and in van der Hoeve de Kleyn's syndrome].
    Cada K, Soudek D.
    Cesk Otolaryngol; 1968 Oct; 17(5):285-7. PubMed ID: 5727172
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  • 5. Cytogenetic study of otosclerosis.
    François J, Matton-Van Leuven MT, Kluyskens P.
    Acta Genet Med Gemellol (Roma); 1967 Apr; 16(2):124-58. PubMed ID: 6062733
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  • 7. [Van der Hoeve syndrome associated with heredity achondroplasia in a psychopath].
    SACERDOTI G, CARRAI E.
    Rass Neuropsichiatr; 1951 Apr; 5(4):227-43. PubMed ID: 13177964
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  • 8. Loss of hearing following the syndrome of Van der Hoeve-de Kleyn.
    Opheim O.
    Acta Otolaryngol; 1968 Mar; 65(3):337-44. PubMed ID: 5653464
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  • 9. Surgical and histological findings of the stapes associated with Van der Hoeve syndrome in a Japanese boy.
    Morimitsu T, Hayashida K.
    ORL J Otorhinolaryngol Relat Spec; 1973 Mar; 35(6):342-9. PubMed ID: 4797685
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  • 10. [Van de Hoeve syndrome].
    Aluffi E, Gandolfi G, Astesiano A, Ferrari F.
    Minerva Chir; 1982 Mar 31; 37(6):569-78. PubMed ID: 7088363
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  • 11. Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndrome.
    Reardon PC, Greenstein RM, Howard RO, Gianacopolos EK, Breg WR.
    Am J Med Genet; 1981 Mar 31; 10(2):113-8. PubMed ID: 7315868
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  • 12. [A case of osteogenesis imperfecta (syndrome of Van der Hoeve-de Kleyn)].
    Bardadin T, Michalewski K.
    Reumatologia; 1969 Mar 31; 7(2):175-80. PubMed ID: 5360577
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  • 14. [Case of osteogenesis imperfecta tarda (Ekman-Lobstein-van der Hoeve-de Kleyn syndrome)].
    Wysocka K, Kiczak J, Daniel B, Zelachowska M.
    Wiad Lek; 1976 Nov 01; 29(21):1937-41. PubMed ID: 997519
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  • 15. [Chromosome mosaicism in the trisomy D syndrome].
    Toledo SP, Wanjtal A.
    Rev Hosp Clin Fac Med Sao Paulo; 1977 Aug 01; 32(4):238-43. PubMed ID: 605335
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  • 18. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M, Visedo G, Sanchís A, Sentís C, Villa A, Ludeña P, Hortigüela JL, Martínez-Frías ML, Fernández-Piqueras J.
    Am J Med Genet; 1994 Jan 01; 49(1):77-82. PubMed ID: 8172255
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  • 19. [Patau syndrome with unusual chromosomal features].
    Friend K, Goldberg MD, Rosenblatt M.
    Harefuah; 1983 Apr 01; 104(7):279-80. PubMed ID: 6618329
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  • 20. Scanning electron microscopy images and energy-dispersive X-ray microanalysis of the stapes in otosclerosis and Van der Hoeve syndrome.
    Vallejo-Valdezate LA, Martín-Gil J, José-Yacamán M, Martín-Gil FJ, Gil-Carcedo LM.
    Laryngoscope; 2000 Sep 01; 110(9):1505-10. PubMed ID: 10983951
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