Observation on the epidemiology, genetics and pathogenesis of deafness in children and lower mammals

References

• Alexander G. Zur vergleichenden, pathologischen Anathomie des Gehörorganes. I. Gehörorgan und Gehirm einer unvollkommen albinotischen, weissen Katze. Arch, Ohrenheilk. 1900; 50: 159–181
   Google Scholar
• Bargman G. J., Gardner L. I. Otic lesions and congenial hypothyroidism in the developing chick. J. clin. Invest. 1967; 46: 1828–1839
   PubMed Web of Science ®Google Scholar
• Bosher S. K., Hallpike C. S. Observations on the histogenesis of the inner ear degeneration of the deaf white cat and its possible relationship to the aetiology of certain unexplained varieties of human congenital deafness. J. Laryng. 1966; 80: 222–235
   PubMedGoogle Scholar
• Brown K. S. Genetic and environmental factors in profound prelingual deafness. Med. Clin. N. Amer. 1969; 53: 741–772
   PubMed Web of Science ®Google Scholar
• Brown K. S., Bergsma D. R., Barrow M. V. Animal models of pigment and hearing abnormalities in man. Presented at the Second Conference on the Clinical Delineation of Birth Defects, The Johns Hopkins Medical Institution. May 26-30, 1969, (in press)
   Google Scholar
• Brown K. S., Chung C. S. Genetic studies of deafness at the Clarke School for the Deaf, Northampton, Mass. Proc. Int. Congr. On Education of the Deaf. U.S. Government Printing Office, Washington 1964; 643–64
   Google Scholar
• Brown K. S., Gordon B., Cavonius C. R. Cochlear function and deafness: Microphonic potentials from skin predict inner ear defects in cats. Nature, Lond., (in press)
   Google Scholar
• Carter C. O. The genetics of common malformations. Progr. med. Genet. Vol. IV. Grune & Stratton, New York 1965; 59–8
   Google Scholar
• Chung C. S. Application of digital computer in human genetics. Meth. Inform. Med. 1964; 3: 67–72
   PubMedGoogle Scholar
• Chung C. S., Brown K. S. Family studies on early childhood deafness ascertained through the Clarke School for the Deaf. Amer. J. hum. Genet., (in press)
   Google Scholar
• Chung C. S., Robison O. W., Morton N. E. A note on deafmutism. Ann. hum. Genet. 1959; 23: 357–366
   PubMed Web of Science ®Google Scholar
• Darwin C. The variation of animals and plants under domestication, vol. II, 2nd ed. Appleton & Co., New York 1892; 322–32
   Google Scholar
• Deol M. S. The origin of the acoustic ganglion and effect of the gene dominant spotting (WV) in the mouse. J. Embryol. Exp. Morph. 1970; 23: 773–784
   PubMedGoogle Scholar
• Falconer D. S. Introduction on quantitative genetics. Ronald Press, New York 1960
   Google Scholar
• Fisch L. Deafness as part of an hereditary syndrome. J. Laryng. 1959; 73: 355–382
   PubMedGoogle Scholar
• Fitzpatrick T.B, Quevedo W. C., Jr. Alninism, in Stanbury; Wyngaarden, and Fedrickson The metabolic basis of inherited disease, 2nd ed. McGraw-Hill), New York 1966
   Google Scholar
• Fraser G. R. Profound childhood deafness. J. med. Genet. 1964; 1: 118–151
   PubMedGoogle Scholar
• Fraser G. R. Sex linked recessive congenital deafness and the excess of males in profound childhood deafness. Ann. hum. Genet. 1965; 29: 171–196
   PubMed Web of Science ®Google Scholar
• Furusho T. A genetic study on the congenital deafness. Jap. J. Human Genet. 1957; 2: 35–58
   Google Scholar
• Hollander C. S. Congenital deafness and goiter. Amer. J. Med. 1964; 37: 630–637
   PubMedGoogle Scholar
• Hopkins L. A. Studies on the inheritance of deafness in the pupils of the Clarke School for the Deaf. Laryngoscope 1946; 56: 570–601
   Google Scholar
• Kittel G., Schmoll-Eskuche G. Statisticshe Erhebungen für Ätiologic ererbter und früh erworbener hochgradiger Perzeptionsstörungen. Arch. Ohr. Nas.-KehlkHeilk. 1963; 181: 310–328
   PubMedGoogle Scholar
• Lumio, Jaakko S., Paljakka Pertti. Tutkimuksia Suomen Kuurojenkeskisista Avioliitoista (Studies on Marriages Between Deaf People in Finland). Duodecim, Suppl. XLIII
   Google Scholar
• Morton N. E. Segregation linkage; in Burdette Methodology in human genetics. Holdon-Day, San Francisco 1962
   Google Scholar
• Neel J. V., Hamilton H. B., Kobara T. Y., Ozaki K. The uneven distribution in Japan of carriers in rare recessive gene causing Acatalasemia and the implication for studies on inbreeding effects; in Goldschmidt The genetics of migrant and isolate populations. Williams and Wilkins, Baltimore 1963
   Google Scholar
• Pendred V. Deaf-mutism and goiter. Lancet 1896; ii: 532
   Google Scholar
• Ross M. D. The general visceral efferent component of the eighth cranial nerve. J. comp. Neurol. 1969; 135: 453–478
   PubMed Web of Science ®Google Scholar
• Sank D. Genetic aspects of early total deafness; in Rainer Family and mental health problems in deaf population. Columbia University, New York 1963
   Google Scholar
• Stevenson A. C., Cheeseman E. A. Hereditary deaf-mutism with special reference to Northern Ireland. Ann. hum. Genet. 1956; 20: 177–207
   PubMed Web of Science ®Google Scholar
• Sugiura A., Hilding D. A. Stria vascularis of deaf hedlund mink. Acta Otolaryng 1970; 69: 160–171
   PubMedGoogle Scholar
• Thould A. K., Scowen E. F. The syndrome of congenital deafness and simple goiter. J. Endocrin. 1964; 30: 69–77
   PubMedGoogle Scholar
• Wakeford O. S., Cavonius C. R., Brown K. S. Measurement of auditory thresholds in the cat using positive reinforcement. Proc. 75th Annual convent. APA 1967; 99–100
   Google Scholar
• Weston J. A. The migration and differentiation of neural crest cells. Adv. morphogenes. 1969; 8: 41–144
   Google Scholar
• Wever E. G. Electrical potentials of the cochlea. Physiol. Rev. 1966; 46: 102–127
   Web of Science ®Google Scholar
• Wilson T. G., Kane F. Congenital deafness in white cats. Acts oto-larying. Stockh. 1958; 50: 269–277
   Google Scholar
• Witkop C. J., Jr., Nance W. E., Rawls R. F., White J. G. Autosomal recessive oculosutaneous albinism in man: Evidence for genetic heterogeneity. Amer. J. hum. Genet. 1970; 22: 55–74
   PubMed Web of Science ®Google Scholar
• Wolff D. Three generations of deaf white cats. J. Hered. 1942; 33: 39–43
   Google Scholar
• World Health Organization. The prevalence of blindness and deafmutism in various countries. Epidemiological Vital Statistics Report 1953; 6: 1–32
   Google Scholar