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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1945 1
1946 2
1947 4
1948 3
1949 2
1950 4
1951 8
1952 5
1953 4
1954 3
1955 2
1956 3
1959 8
1960 3
1961 11
1962 3
1963 12
1964 33
1965 35
1966 30
1967 35
1968 57
1969 64
1970 76
1971 85
1972 57
1973 72
1974 101
1975 91
1976 92
1977 106
1978 80
1979 53
1980 45
1981 53
1982 41
1983 63
1984 69
1985 69
1986 64
1987 55
1988 64
1989 57
1990 72
1991 93
1992 73
1993 90
1994 87
1995 99
1996 89
1997 121
1998 123
1999 161
2000 192
2001 195
2002 195
2003 155
2004 170
2005 171
2006 175
2007 232
2008 235
2009 212
2010 300
2011 276
2012 305
2013 313
2014 341
2015 358
2016 370
2017 363
2018 360
2019 387
2020 436
2021 496
2022 546
2023 567
2024 199

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9,247 results

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Quoted phrase not found in phrase index: "Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness"
Page 1
Waardenburg syndrome.
Tagra S, Talwar AK, Walia RL, Sidhu P. Tagra S, et al. Indian J Dermatol Venereol Leprol. 2006 Jul-Aug;72(4):326. doi: 10.4103/0378-6323.26718. Indian J Dermatol Venereol Leprol. 2006. PMID: 16880590
Molecular diagnosis of hereditary deafness and application of stepwise testing strategy.
Zeng BP, Xu HG, Mao L, Tang WX. Zeng BP, et al. Yi Chuan. 2023 Jan 20;45(1):29-41. doi: 10.16288/j.yczz.22-206. Yi Chuan. 2023. PMID: 36927636 Review.
Hereditary deafness is one of the most common sensory disorders in humans, and exhibits high genetic heterogeneity. ...In this review, we evaluate and discuss the utility of molecular diagnosis and the application of stepwise testing strategies in hereditary deafness …
Hereditary deafness is one of the most common sensory disorders in humans, and exhibits high genetic heterogeneity. ...In this review …
Why American Sign Language Gloss Must Matter.
Supalla SJ, Cripps JH, Byrne AP. Supalla SJ, et al. Am Ann Deaf. 2017;161(5):540-551. doi: 10.1353/aad.2017.0004. Am Ann Deaf. 2017. PMID: 28238974 Review.
Branchio-oto-renal syndrome.
Garg A, Wadhera R, Gulati SP, Kumar A. Garg A, et al. J Assoc Physicians India. 2008 Nov;56:904-5. J Assoc Physicians India. 2008. PMID: 19263692
Authors are reporting a 19 year male patient, who presented with profound deafness & low set "lop-ear" with right sided preauricular pit. USG abdomen revealed agenesis of the left kidney....
Authors are reporting a 19 year male patient, who presented with profound deafness & low set "lop-ear" with right sided preauricu …
Word-deafness revisited.
[No authors listed] [No authors listed] Lancet. 1986 Jun 28;1(8496):1477-8. Lancet. 1986. PMID: 2873285 No abstract available.
Deafness in the genomics era.
Shearer AE, Hildebrand MS, Sloan CM, Smith RJ. Shearer AE, et al. Hear Res. 2011 Dec;282(1-2):1-9. doi: 10.1016/j.heares.2011.10.001. Epub 2011 Oct 8. Hear Res. 2011. PMID: 22016077 Free PMC article. Review.
Our understanding of hereditary hearing loss has greatly improved since the discovery of the first human deafness gene. These discoveries have only accelerated due to the great strides in DNA sequencing technology since the completion of the human genome project. Here, we …
Our understanding of hereditary hearing loss has greatly improved since the discovery of the first human deafness gene. These discove …
Brain Plasticity and Rehabilitation with a Cochlear Implant.
McKay CM. McKay CM. Adv Otorhinolaryngol. 2018;81:57-65. doi: 10.1159/000485586. Epub 2018 Apr 6. Adv Otorhinolaryngol. 2018. PMID: 29794427 Review.
The functional changes that occur in the brain due to deafness may affect the way the auditory system processes sound after cochlear implantation. ...The functional plasticity that occurs in postlingually deaf adults during periods of deafness can both support and h …
The functional changes that occur in the brain due to deafness may affect the way the auditory system processes sound after cochlear …
The usher syndromes.
Keats BJ, Corey DP. Keats BJ, et al. Am J Med Genet. 1999 Sep 24;89(3):158-66. Am J Med Genet. 1999. PMID: 10704190 Review.
MYO7A is on chromosome region 11q13 and USH2A is on 1q41. Seven other USH genes have been mapped but have not yet been identified. USH1A, USH1C, USH1D, USH1E, and USH1F have been assigned to chromosome bands 14q32, 11p15.1, 10q, 21q21, and 10, respectively, while USH2B is …
MYO7A is on chromosome region 11q13 and USH2A is on 1q41. Seven other USH genes have been mapped but have not yet been identified. US …
Deafness: diagnosis and management.
Tonkin JP. Tonkin JP. Med J Aust. 1990 Jun 18;152(12):659-63. doi: 10.5694/j.1326-5377.1990.tb125426.x. Med J Aust. 1990. PMID: 2198446 Review. No abstract available.
9,247 results