References
- Altmann F. Histologic pictures of inherited nerve deafness. Arch. Otolaryng. (Chic) 1950; 51: 852
- Altmann F. Malformations, anomalies, and vestigial structures of the inner car. Arch. Otolaryng. (Chic) 1953; 57: 591
- Altmann F. The inner ear in genetically determined deafness. Acta Otolaryng. (Stockh.) 1964, Suppl. 187
- Arnvig J. Vestibular function in deafness and severe hardness of hearing. Acta Otolaryng. (Stockh.) 1955; 45: 283
- Evekherg G. Etiology of unilateral total deafness. Ann. Otol. 1960a; 69: 711
- Evekherg G. Investigations into unilateral deafness and absence of vestibular function with a particular view to the X-ray appearances in the inner ear. Acta Otolaryng. (Stockh.) 1960b; 52: 47
- Evekherg G. Further studies on hereditary unilateral deafness. Acta Otolaryng. (Stockh.) 1960c; 51: 615
- Evekherg G. Knsidig dcivhed. Thesis, Copenhagen 1961
- Evekherg G. Congenital obliterations of the semicircular canals. Ann. Laringol. Otol. Faringol. 1962; 61: 5
- Everberg G., Ratjen E., Sörensen H. Wildervanck's syndrome. Klippel Feil's syndrome associated with deafness and retraction of the eyeball. Brit. J. Radiol. 1963a; 36: 562
- Everberg G., Ratjen E., Sörensen H. Unilateral atresia of the internal auditory meatus, confirmed by radiography. Brit. J. Radiol. 1963b; 36: 568
- Fisch L. Deafness as a part of an hereditary syndrome. J. Laryng. 1959; 73: 355
- Franceschetti A., Klein D. Dysmorphic cervico-oculo-faciale avee surditReA fainliale. J. Génét. Hum. 1954; 3: 176
- Fraser G. It. Profound childhood deafness. J. Med. Genet. 1964; 1: 137
- Fraser G. It. Association of congenital deafness with goitre (Pendred's syndrome). Ann. Hum. Genet. 1965; 28: 201
- Fhaser G. R., Frogatt P., James T. N. Congenital deafness associated with electrocardiographic abnormalities, fainting attacks and sudden death. Quart. J. Med. 1964; 33: 361
- Grimaud R., Mounier-Kuhn P., Gignoux M., Martin H. Troubles de l'appareil auditif et manifestations ophtalmologiques associées. Soc. Franç. d'Oto-Rhino- Larynij, Paris 1962
- Guli E., Bonetti U. Vol. Hered. Pathol. 1956; 5: 101
- Hanhart E. Die genealogische und otologische Erforschung des grossen Walliser Hordes von rezessiver Taubheit und Schwerhörigkeit im Laufe der Ictzten 30 Jalire (1933–1962). Arch. Klaus-Stift. Vererb. Forsch. 1962; 37: 196
- Johnsen S., Fueiesleben I. The relation between erythroblastosis foetalis, Uernictcrus and impairment of hearing. Ada Otolaryng. (Stockh.) 1952; 42: 35
- Leiber B., Olbrich G. Wörterbuch der klinischen Syndrome3rd ed. 1963; 645
- Lindenov H. The Etiology of Deaf-Mutism. Copenhagen 1945
- Ohmekod F. C. (1960) The pathology of congenital deafness in the child. Rep. Inf. Conyr. Modern Educat. Treatment Deafness, Manchester, 1958, 8
- Ohmekod F. C. The pathology of congenital deafness. J. Laryng. 1960; 74: 919
- Pintucci F., di Tizio A. Dysmorphie cervico-oculo-faciale. J. Génét. Hum. 1961; 10: 156
- Sécrétan J. P. De la surdi-mutite recessive et de ses rapports avec les autres formes de surdi-mutité. Arch. Klaus-Stift. Vererb. Forsch. 1954; 29: 1
- Siebenmann F., Bing H. tiber den Labyrinth- und Hirnbefund bei einem an Retinitis pigmentosa erblindeten z angeborenen Taubstummen. Z. Ohrenheilk. 1907; 54: 265
- Thorkilgaahd O. Waardenburg's syndrome in father and daughter. Acta Ophthalm. 1962; 40: 590
- Waahdenburg P. J. A new syndrome. Amer. J. Hum. Genet. 1951; 3: 195
- Waahdenburg P. J. Genetics and Ophthalmology, P. Waardenburg, A. Franceschetti, D. Klein, AssenNetherlands 1961–1963; I: 428, 431–433, and II, 1118, 1123
- Whetnall E., Fry D. B. The Deaf Child. London 1964; 103
- Wildervanck L. S. Een geval van aandoening van Klippel-Feil gecombiiieerd met abducens paralyse, retractio bulbi en doofstomheid. Ned. T. Geneesk. 1952; 96: 2752
- Wildervanck L. S. Ken cervico-oculo-acusticus syndroom. Ned. T. Geneesk. 1960; 10b: 2600
- Wildervanck L. S. Hereditary syndromes in conductive and perceptive deafness. I'roc. Sec. Internal. Course Paedo-audiol, Groningen 1961; 90
- Wildervanck L. S. (1963a) A cervico-oculo-acusticus syndrome belonging to the status dysraphicus. Proc. Sec. lnternat. Conyr. Hum. Genet., Rome, 1961. III: 1409
- Wildervanck L. S. Perceptive deafness associated with splithand and -foot, a new syndrome. Acta Genet. (Basel) 1963b; 13: 161
- Wildervanck L. S. (1964) The significance of associated anomalies in deafness. Rep. I'roc. Int. Conyr. Educat. of the Deaf. 1963. Gallaudet College, Washington, DC, 632