-
1
-
-
0026410464
-
Genetic epidemiology of hearing impairment
-
Morton N E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci 1991; 630: 16–31
-
(1991)
Ann N Y Acad Sci
, vol.630
, pp. 16-31
-
-
Morton, N.E.1
-
2
-
-
0027180952
-
Genetic epidemiological studies of early-onset deafness in the U.S. school-age population
-
Marazita M L, Ploughman L M, Rawlings B, Remington E, Arnos K S, Nance W E. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population. Am J Med Genet 1993; 46: 486–91
-
(1993)
Am J Med Genet
, vol.46
, pp. 486-491
-
-
Marazita, M.L.1
Ploughman, L.M.2
Rawlings, B.3
Remington, E.4
Arnos, K.S.5
Nance, W.E.6
-
3
-
-
0028227613
-
Nonsyndromic hearing loss: an analysis of audiograms
-
Liu X, Xu L. Nonsyndromic hearing loss: an analysis of audiograms. Ann Otol Rhinol Laryngol 1994; 103: 428–33
-
(1994)
Ann Otol Rhinol Laryngol
, vol.103
, pp. 428-433
-
-
Liu, X.1
Xu, L.2
-
4
-
-
0030946546
-
Nonsyndromic hearing impairment: unparalleled heterogeneity
-
Van Camp G, Willems P J, Smith R JH. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 1997; 60: 758–64
-
(1997)
Am J Hum Genet
, vol.60
, pp. 758-764
-
-
Van Camp, G.1
Willems, P.J.2
Smith, R.J.H.3
-
6
-
-
0019426002
-
Low frequency hereditary deafness in man with childhood onset
-
León P E, Bonilla J A, Sánchez Al. Low frequency hereditary deafness in man with childhood onset. Am J Hum Genet 1981; 33: 209–14
-
(1981)
Am J Hum Genet
, vol.33
, pp. 209-214
-
-
León, P.E.1
Bonilla, J.A.2
Sánchez, A.3
-
7
-
-
0026695288
-
The gene for an inherited form of deafness maps to chromosome 5q31
-
León P E, Raventos H, Lynch E, Morrow J, King M-C. The gene for an inherited form of deafness maps to chromosome 5q31. Proc Natl Acad Sci USA 1992; 89: 5181–4
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 5181-5184
-
-
León, P.E.1
Raventos, H.2
Lynch, E.3
Morrow, J.4
King, M.-C.5
-
8
-
-
0028101878
-
Linkage of autosomal dominant hearing loss to tile short arm of chromosome 1 in two families
-
et al
-
Coucke P, Van Camp G, Djoyodiharjo B, et al. Linkage of autosomal dominant hearing loss to tile short arm of chromosome 1 in two families. N Engl J Med 1994; 331: 425–31
-
(1994)
N Engl J Med
, vol.331
, pp. 425-431
-
-
Coucke, P.1
Van Camp, G.2
Djoyodiharjo, B.3
-
10
-
-
0030917967
-
Inherited nonsyndromic hearing loss. An audio-vestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2
-
et al
-
Marres H, Van Ewijk M, Huygen P, et al. Inherited nonsyndromic hearing loss. An audio-vestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2. Arch Otolaryngol Head Neck Surg 1997; 123: 573–7
-
(1997)
Arch Otolaryngol Head Neck Surg
, vol.123
, pp. 573-577
-
-
Marres, H.1
Van Ewijk, M.2
Huygen, P.3
-
11
-
-
0031962461
-
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: Audiologic analysis of a pedigree linked to DFNA2
-
et al
-
Kunst H, Marres H, Huygen P, et al. Nonsyndromic autosomal dominant progressive sensorineural hearing loss: Audiologic analysis of a pedigree linked to DFNA2. Laryngoscope 1998; 108: 74–80
-
(1998)
Laryngoscope
, vol.108
, pp. 74-80
-
-
Kunst, H.1
Marres, H.2
Huygen, P.3
-
12
-
-
0013864374
-
Studies on progressive hereditary perceptive deafness in a family of 335 members. I. Genetical and general audiological results
-
Huizing E H, Van Bolhuis A H, Odenthal D W. Studies on progressive hereditary perceptive deafness in a family of 335 members. I. Genetical and general audiological results. Acta Otolaryngol 1966; 61: 35–41
-
(1966)
Acta Otolaryngol
, vol.61
, pp. 35-41
-
-
Huizing, E.H.1
Van Bolhuis, A.H.2
Odenthal, D.W.3
-
13
-
-
0013862487
-
Studies on progressive hereditary perceptive deafness in a family of 335 members. II. Characteristic pattern of hearing deterioration
-
Huizing E H, Van Bolhuis A H, Odenthal D W. Studies on progressive hereditary perceptive deafness in a family of 335 members. II. Characteristic pattern of hearing deterioration. Acta Otolaryngol 1966; 61: 161–7
-
(1966)
Acta Otolaryngol
, vol.61
, pp. 161-167
-
-
Huizing, E.H.1
Van Bolhuis, A.H.2
Odenthal, D.W.3
-
14
-
-
0001562385
-
Results of further studies on progressive hereditary sensorineural hearing loss
-
Huizing E H, Van Bolhuis A H, Odenthal D W. Results of further studies on progressive hereditary sensorineural hearing loss. Audiology 1972; 12: 261–3
-
(1972)
Audiology
, vol.12
, pp. 261-263
-
-
Huizing, E.H.1
Van Bolhuis, A.H.2
Odenthal, D.W.3
-
17
-
-
0021838244
-
Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. I. Analysis of hearing deterioration
-
Van den Wijngaart W SIM, Huizing E H, Niermeijer M F, Verschuure J, Brocaar M P, Blom W. Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. I. Analysis of hearing deterioration. Audiology 1985; 24: 233–40
-
(1985)
Audiology
, vol.24
, pp. 233-240
-
-
Van den Wijngaart, W.S.I.M.1
Huizing, E.H.2
Niermeijer, M.F.3
Verschuure, J.4
Brocaar, M.P.5
Blom, W.6
-
18
-
-
0021929875
-
Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. II. Clinical aspects
-
Van den Wijngaart W SIM, Huizing E H, Niermeijer M F, Verschuure J, Brocaar M P, Blom W. Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. II. Clinical aspects. Audiology 1985; 24: 336–42
-
(1985)
Audiology
, vol.24
, pp. 336-342
-
-
Van den Wijngaart, W.S.I.M.1
Huizing, E.H.2
Niermeijer, M.F.3
Verschuure, J.4
Brocaar, M.P.5
Blom, W.6
-
19
-
-
0028803173
-
Localizations of a locus for non-syndromic hearing loss (DFNA5) to chromosome 7p
-
et al
-
Van Camp G, Coucke P, Dalemans W, et al. Localizations of a locus for non-syndromic hearing loss (DFNA5) to chromosome 7p. Hum Mol Genet 1995; 4: 2159–63
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2159-2163
-
-
Van Camp, G.1
Coucke, P.2
Dalemans, W.3
-
20
-
-
0014333011
-
Dominantly inherited low-frequency hearing loss
-
The Vanderbilt University Hereditary Deafness Study Group. Dominantly inherited low-frequency hearing loss. Arch Otolaryngol 1968; 88: 242–50
-
(1968)
Arch Otolaryngol
, vol.88
, pp. 242-250
-
-
-
21
-
-
0038627226
-
-
Book of abstracts p
-
Hall J W, III, Bess F, Strouse A, Chase P. Dominant inherited low frequency hearing loss: documentation in five generations. XXII International Congress of Audiology. Halifax, Nova Scotia, Canada. July 3-8. 1994; 102, Book of abstracts p
-
(1994)
Dominant inherited low frequency hearing loss: documentation in five generations. XXII International Congress of Audiology. Halifax, Nova Scotia, Canada. July 3-8
, pp. 102
-
-
Hall, J.W.1
Bess, F.2
Strouse, A.3
Chase, P.4
-
22
-
-
0028892097
-
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4pl6.3
-
et al
-
Lesperance M M, Hall J W, Bess F H, et al. A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4pl6.3. Hum Mol Genet 1995; 4: 1967–72
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1967-1972
-
-
Lesperance, M.M.1
Hall, J.W.2
Bess, F.H.3
-
23
-
-
0031926717
-
Review of non-syndromic autosomal dominant sensorineural hearing loss: a new field of research
-
Kunst H, Marres H, Van Camp G, Cremers C. Review of non-syndromic autosomal dominant sensorineural hearing loss: a new field of research. Clin Otolaryngol 1998; 23: 9–17
-
(1998)
Clin Otolaryngol
, vol.23
, pp. 9-17
-
-
Kunst, H.1
Marres, H.2
Van Camp, G.3
Cremers, C.4
-
24
-
-
0003803339
-
-
November
-
European Work Group on Genetics of Hearing Impairment. Infoletter 2. 1996, November
-
(1996)
Infoletter 2
-
-
-
28
-
-
0018779147
-
Age effect in hearing–a comparative analysis of published threshold data
-
Robinson D W, Sutton G J. Age effect in hearing–a comparative analysis of published threshold data. Audiology 1979; 18: 320–34
-
(1979)
Audiology
, vol.18
, pp. 320-334
-
-
Robinson, D.W.1
Sutton, G.J.2
-
29
-
-
0026667822
-
Oculomotor, auditory, and vestibular responses in myotonic dystrophy
-
Verhagen W IM, Ter Bruggen J P, Huygen P LM. Oculomotor, auditory, and vestibular responses in myotonic dystrophy. Arch Neurol 1992; 49: 954–60
-
(1992)
Arch Neurol
, vol.49
, pp. 954-960
-
-
Verhagen, W.I.M.1
Ter Bruggen, J.P.2
Huygen, P.L.M.3
-
31
-
-
0027511172
-
Constructive interference in steady state (CISS)-3D FT MR imaging of the inner ear and cerebellopontine angle
-
Casselman J W, Kuhweide R, Deimling M, Ampe W, Dehaene I, Meeus L. Constructive interference in steady state (CISS)-3D FT MR imaging of the inner ear and cerebellopontine angle. Am J Neuroradiol 1993; 14: 47–57
-
(1993)
Am J Neuroradiol
, vol.14
, pp. 47-57
-
-
Casselman, J.W.1
Kuhweide, R.2
Deimling, M.3
Ampe, W.4
Dehaene, I.5
Meeus, L.6
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