Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis

References

• Cottingham RW Jr, Idury RM, Schaffer AA. Faster sequential genetic linkage computations. Am J Hum Genet 1993;53:252–63.
   PubMed Web of Science ®Google Scholar
• Elberling C, Ludvigsen C, Lyregaard PE. DANtale. A new Danish speech material. Scand Audiol 1989;18: 169–75.
   PubMed Web of Science ®Google Scholar
• Gates GA, Couropmitree NN, Myers RH. Genetic associations in age-related hearing thresholds. Arch Otolaryngol Head Neck Surg 1999;125:654–9.
   PubMedGoogle Scholar
• HEAR: European Work Group on Genetics of Hearing Impairment. Infoletter 2. November 1996.
   Google Scholar
• ISO 389–3 Acoustics -Reference Zero for the calibra-tion of audiometric equipment. Geneva: International Organization for Standardization, 1994.
   Google Scholar
• ISO 8253–1 Acoustics - Audiometric test methods. Part 1. Basic pure-tone air and bone conduction threshold audiometry. Geneva: International Organization for Standardization, 1989.
   Google Scholar
• Jenkins HA, Morgan DE, Miller RH. Intact acoustic reflexes in the presence of ossicular disruption. Laryngoscope 1980;90:267–73.
   Google Scholar
• Jerger J. Diagnostic audiometry. In: Jerger J, ed. Modern developments in audiology. New York: Aca-demic Press, 1973.
   Google Scholar
• Karlsson KK, Harris JR, Svartengren M. Description and primary results from an audiometric study of male twins. Ear Hear 1997;18:114–20.
   Google Scholar
• Khanna SM, Tonndorf J, Queller JE. Mechanical parameters of hearing by bone conduction. J Acoust Soc Am 1976;60:139–54.
   PubMed Web of Science ®Google Scholar
• Königsmark BW, Mengel M, Berlin CI. Familial low frequency hearing loss. Laryngoscope 1971;81:759–71.
   PubMed Web of Science ®Google Scholar
• Kunst H, Manes H, Huygen P, Van Camp G, Joosten F, Cremers C. Autosomal dominant non-syndromal low-frequency hearing impairment linked to chromosome 4p16 (DFNA14): Statistical analysis of hearing thresh-old in relation to age and evaluation of vestibulo-ocular functions. Audiology 1999;38: 165–73.
   Google Scholar
• Lalwani AK, Jackler JK, Sweetow RW et al. Further characterization of the DFNA1 audiovestibular pheno-type. Arch Otolaryngol Head Neck Surg 1998;124:699–702.
   PubMed Web of Science ®Google Scholar
• Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36:460–5.
   PubMed Web of Science ®Google Scholar
• Leon PE, Bonilla JA, Sanchez JR et al. Low frequency hereditary deafness in man with childhood onset. Am J Hum Genet 1981;33:209–14.
   PubMed Web of Science ®Google Scholar
• Leon PE, Raventos H, Lynch E, Morrow J, King MC. The gene for an inherited form of deafness maps to chromosome 5q31. Proc Natl Acad Sci 1992;89: 5181–4.
   Google Scholar
• Lesperance MM, Hall JW, Bess FH et al. A gene for autosomal dominant nonsyndomic hereditary hearing impairment maps to 4p16.3. Hum Mol Genet 1995;4: 1967–72.
   PubMed Web of Science ®Google Scholar
• Lynch ED, Lee MK, Morrow JE, Welcsh PL, Leon PE, King MC. Nonsyndromic deafness DFNA1 associated with mutation of the human homolog of the Drosophila gene diaphanous. Science 1997;278:1315–8.
   PubMed Web of Science ®Google Scholar
• Martini A, Milani M, Rosignoli M, Mazzoli M, Prosser S. Audiometric patterns of genetic non-syndromal sensorineural hearing loss. Audiology 1997;36:228–36.
   Google Scholar
• Martini A, Prosser S. Audiometric patterns of genetic hearing loss. In: Martini A, Read A, Stephens D, eds. Genetics and hearing impairment. London: Whurr Publishers Ltd, 1996:92–9.
   Google Scholar
• Olsen S. Evaluation of the lists of numerals in the Danish speech audiometry material: DANtale. Scand Audiol 1996;25:103–7.
   PubMed Web of Science ®Google Scholar
• Parving A. Inherited low-frequency hearing loss. A new mixed conductive/sensorineural entity? Scand Audiol 1984;13:47–56.
   PubMedGoogle Scholar
• Parving A, Bak-Pedersen K. Clinical findings and diagnostic problems in sensorineural low frequency hearing loss. Acta Otolaryngol 1978;85:184–90.
   PubMed Web of Science ®Google Scholar
• Parving A, Elberling C. High-pass masking in the classification of low-frequency hearing loss. Scand Audiol 1982;11:173–8.
   PubMed Web of Science ®Google Scholar
• Parving A, Johnsen NJ, Holm-Jensen S. Dominantly inherited low-frequency hearing loss. Audiology 1978; 17:165–72.
   Google Scholar
• Parving A, Sakihara Y, Christensen B. Inherited sensorineural low-frequency hearing impairment: some aspects of phenotype and epidemiology. Audiol-ogy 2000;39:50–60.
   Google Scholar
• Snik AF, Hombergen GC, Mylanus EA, Cremers CW. Airborne gap in patients with X-linked stapes gusher syndrome. Am J Otol 1995;16:241–6.
   PubMedGoogle Scholar
• The Vanderbilt University Hereditary Deafness Study Group. Dominantly inherited low-frequency hearing loss. Arch Otolaryngol 1968;88:242–50.
   PubMed Web of Science ®Google Scholar
• Van Camp G, Kunst H, Flothmann K et al. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. J Med Genet 1999;36:532–6.
   Google Scholar
• Van Camp G, Smith RJH. Hereditary Hearing Loss Homepage. World Wide Web, Marts 2001. URL:http:// www.uia.ac.be/dnalab/hhh/
   Google Scholar
• Wilton JF, Erway LC. Genetics of age-related hearing loss in mice. IV. Cochlear pathology and hearing loss in 25 BXD recombinant inbred mouse strains. Hear Res 1998;119:27–36.
   Google Scholar