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Hauptvortrag II

  • Conference paper
Teil II: Sitzungsbericht

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Zusammenfassung

Um das Interesse und die Bedeutung der HNO-Heilkunde und der Humangenetik füreinander zu charakterisieren, sollen 3 Aussagen und ihre Gegensätze konstruiert werden. Sie orientieren sich an der Gehörlosigkeit als einem bekannten und typischen Beispiel. Dieses hat eine erhebliche, ebenso individuelle wie soziale Bedeutung, und das Problem der Gehörlosen beschäftigt seit langem den Arzt und die Gesellschaft.

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Literatur

  1. Aase JM (1980) Microtia — Clinical observations. BOAS XVI, 4: 289–297

    Google Scholar 

  2. Ammermann M, Pfeiffer RA, Hüther W, Becker R (1971) Zur Frage der Vererbung der Dysostosis mandibulo-facialis. Munch Med Wochenschr 113: 1686–1690

    PubMed  CAS  Google Scholar 

  3. Costeff H, Dar H (1980) Consanguinity analysis of congenital deafness in Northern Israel. Am J Human Genet 32: 64–68

    CAS  Google Scholar 

  4. De La Cruz E, Sun S, Vangvanichyakorn K, Desposito F (1984) Multiple congenital malformations associated with maternal isoretinoin therapy. Pediatrics 74: 428–430

    PubMed  Google Scholar 

  5. Ernst M, Schilbach U (1987) Hypo/Aplasie der Nasenbeine — eine autosomal dominant vererbte Anomalie. HNO 35: 478–481

    PubMed  CAS  Google Scholar 

  6. Fraser GR (1976) The causes of profound deafness in childhood. Johns Hopkins Univ Press, Baltimore

    Google Scholar 

  7. Friend StH, Dryja PhP, Weinberg RA (1988) Oncogenes and tumor-suppressing genes. N Engl J Med 318: 618–622

    Article  PubMed  CAS  Google Scholar 

  8. Goswami HK (1980) Hairy tip of nose — a new trait in males. Am J Med Genet 5: 259–263

    Article  PubMed  CAS  Google Scholar 

  9. Halal F (1982) Dominant inheritance of nose pits. Am J Med Genet 13: 101–104

    Article  PubMed  CAS  Google Scholar 

  10. Konigsmark BW, Gorlin JW (1976) Genetic and metabolic deafness. Saunders, Philadelphia

    Google Scholar 

  11. Lammer EJ, Chen DT, et al. (1985) Retinoic acid embryopathy. N Engl J Med 313: 837–841

    Article  PubMed  CAS  Google Scholar 

  12. Lander ES, Botstein D (1987) Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science 236: 1567–1570

    Article  PubMed  CAS  Google Scholar 

  13. Lowry RB, Morgan K, Holmes TM, Metcalf PJ, Stauffer EF (1985) Mandibulofacial dysostosis in hutterite sibs: a possible recessive trait. Am J Med Genet 22: 501–512

    Article  PubMed  CAS  Google Scholar 

  14. Lungarotti MS, Marinelli D, Mariani T, Calabro A (1987) Multiple congenital anomalies associated with apparently normal maternal intake of vitamin A: a phenocopy of the isoretinoin syndrome. Am J Med Genet 27: 245–248

    Article  PubMed  CAS  Google Scholar 

  15. Martuza RL, Eldridge R (1988) Neurofibromatosis 2 ( Bilateral acoustic neurofibromatosis ). N Engl J Med 318: 684–688

    Article  PubMed  CAS  Google Scholar 

  16. Melnick M (1980) The etiology of external ear malformations and its relation to abnormalities of the middle ear, inner ear, and other organ systems. BOAS XVI, 4: 303–331

    Google Scholar 

  17. Nance WE (1980) The genetic analysis of profound prelingual deafness. BOAS XVI, 4: 263–269

    Google Scholar 

  18. Nance WE, McConnell FF (1973) Status and prospects of research in hereditary deafness. In: Harris H, Hirschhorn K (eds) Advances in human genetics, vol 4. Plenum Press, New York

    Google Scholar 

  19. Pfeiffer RA (1982) Essai d’une nosologie genetique de l’atresia auris congenita. J Genet Human 30: 165–180

    CAS  Google Scholar 

  20. Schwarz M (1940) Die erbliche Taubheit und ihre Diagnostik. In: Gutt A (Hrsg) Handbuch der Erbkrankheiten, Bd 6. Thieme, Leipzig

    Google Scholar 

  21. Seunaez H, Mane-Garzon F, Kotski R (1976) Cardio-cutaneous syndrome (the “Leopard” Syndrome). Review of the literature and a new family. Clin Genet 9: 266–276

    Article  Google Scholar 

  22. Siniscalco M (1987) On the strategies and priorities for sequencing the human genome: a personal view. Trends Genet 2: 182–184

    Article  Google Scholar 

  23. White R, Lalouel JM (1988) Chromosome mapping with DNA markers. Sci Am 258: 20–28

    Article  Google Scholar 

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Author information

Authors and Affiliations

  1. Erlangen, Deutschland

    R. A. Pfeiffer

Authors
  1. R. A. Pfeiffer
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Editor information

Editors and Affiliations

  1. Universität-HNO-Klinik, Feulgenstr. 10, 6300, Gießen, Deutschland

    Konrad Fleischer

  2. Klinik und Poliklinik für HNO-Kranke, Universität Erlangen-Nürnberg, Waldstr. 1, 8520, Erlangen, Deutschland

    Malte Erik Wigand

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© 1988 Springer-Verlag Berlin Heidelberg

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Pfeiffer, R.A. (1988). Hauptvortrag II. In: Fleischer, K., Wigand, M.E. (eds) Teil II: Sitzungsbericht. Verhandlungsbericht der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie, vol 1988 / 2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-83614-5_9

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  • DOI: https://doi.org/10.1007/978-3-642-83614-5_9

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-50343-9

  • Online ISBN: 978-3-642-83614-5

  • eBook Packages: Springer Book Archive

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