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Journal Abstract Search

129 related items for PubMed ID: 3582212

  • 1. The BOR syndrome as a possible neurocristopathy.
    Gimsing S.
    Ear Nose Throat J; 1987 Apr; 66(4):154-8. PubMed ID: 3582212
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  • 3. Branchio-oto-renal dysplasia and branchio-oto dysplasia: report of eight new cases.
    Martini A, Comacchio F, Candiani F, Vio S.
    Am J Otol; 1987 Mar; 8(2):116-22. PubMed ID: 3591918
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  • 5. [Deafness and hypacusis combined with branchiogenic and sometimes renal congenital abnormalities].
    Cremers CW, Marres EH.
    Ned Tijdschr Geneeskd; 1977 Nov 19; 121(47):1676-9. PubMed ID: 917140
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  • 7. [Clinical and genetic analysis of the Townes-Brocks syndrome].
    Il'ina EG, Laziuk GI.
    Tsitol Genet; 1992 Nov 19; 26(4):32-5. PubMed ID: 1440915
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  • 8. Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.
    Melnick M, Hodes ME, Nance WE, Yune H, Sweeney A.
    Clin Genet; 1978 May 19; 13(5):425-42. PubMed ID: 657583
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  • 10. Lacrimo-auriculo-dento-digital syndrome: a literature review and case reports.
    Toumba KJ, Gutteridge DL.
    Quintessence Int; 1995 Dec 19; 26(12):829-39. PubMed ID: 8596813
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  • 11. Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?
    Fraser FC, Aymé S, Halal F, Sproule J.
    Am J Med Genet; 1983 Mar 19; 14(3):473-8. PubMed ID: 6859100
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  • 13. [Familial multiple congenital anomalies of oto-cervical localization].
    Bochnia M, Swiatkowska M.
    Otolaryngol Pol; 1978 Mar 19; 32(5):517-21. PubMed ID: 714467
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  • 14. Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations.
    Kurnit DM, Steele MW, Pinsky L, Dibbins A.
    J Pediatr; 1978 Aug 19; 93(2):270-3. PubMed ID: 671168
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  • 15. A distinct dominant form of microtia and conductive hearing loss.
    Sánchez-Corona J, García-Cruz D, Ruenes R, Cantú JM.
    Birth Defects Orig Artic Ser; 1982 Aug 19; 18(3B):211-6. PubMed ID: 7139104
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  • 17. Melnick-Fraser syndrome.
    Torres-Peris V, Jorda E, Ramon D, Peiro J, Revert A, Torres-Larrosa T.
    Dermatology; 1994 Aug 19; 189(1):103-4. PubMed ID: 8003778
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  • 18. Autosomal dominant first and second branchial arch syndrome. A new inherited syndrome?
    Karmody CS, Feingold M.
    Birth Defects Orig Artic Ser; 1974 Aug 19; 10(7):31-40. PubMed ID: 4424226
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  • 19. [Hereditary combination of branchial fistulas and middle ear malformations (author's transl)].
    Pau HW, Koch U.
    Laryngol Rhinol Otol (Stuttg); 1979 Jan 19; 58(1):88-95. PubMed ID: 763058
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