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

Year Number of Results
1969 1
1971 3
1972 1
1973 1
1975 1
1976 2
1977 2
1978 4
1979 3
1980 3
1981 3
1982 4
1983 6
1984 3
1985 3
1986 5
1987 4
1988 3
1989 4
1990 4
1991 7
1992 9
1993 8
1994 9
1995 9
1996 10
1997 9
1998 12
1999 14
2000 12
2001 6
2002 11
2003 6
2004 10
2005 4
2006 4
2007 6
2008 11
2009 5
2010 5
2011 5
2012 2
2013 2
2015 1
2016 1
2018 1
2019 1
2022 0
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Article type
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Search Results

233 results
Results by year
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Page 1
Response.
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, Defries JC. Cardon LR, et al. Among authors: kimberling wj. Science. 1995 May 12;268(5212):787-8. doi: 10.1126/science.268.5212.787. Science. 1995. PMID: 17792159 No abstract available.
Branchio-oto-renal syndrome.
Kochhar A, Fischer SM, Kimberling WJ, Smith RJ. Kochhar A, et al. Among authors: kimberling wj. Am J Med Genet A. 2007 Jul 15;143A(14):1671-8. doi: 10.1002/ajmg.a.31561. Am J Med Genet A. 2007. PMID: 17238186 Review.
The inheritance of psoriasis.
Kimberling W, Dobson RL. Kimberling W, et al. J Invest Dermatol. 1973 Jun;60(6):538-40. doi: 10.1111/1523-1747.ep12703617. J Invest Dermatol. 1973. PMID: 4351104 Free article. Review. No abstract available.
Hereditary deafness.
Kimberling WJ. Kimberling WJ. Am J Med Genet. 1999 Sep 24;89(3):121-2. doi: 10.1002/(sici)1096-8628(19990924)89:3<121::aid-ajmg1>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10704185 No abstract available.
Hearing loss disorders associated with renal disease.
Kimberling WJ, Borsa N, Smith RJH. Kimberling WJ, et al. Adv Otorhinolaryngol. 2011;70:75-83. doi: 10.1159/000322478. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358188 Review.
Genetic heterogeneity of Usher syndrome.
Kimberling WJ, Orten D, Pieke-Dahl S. Kimberling WJ, et al. Adv Otorhinolaryngol. 2000;56:11-8. doi: 10.1159/000059077. Adv Otorhinolaryngol. 2000. PMID: 10868209 Review.
Localization of two genes for Usher syndrome type I to chromosome 11.
Smith RJ, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJ, Jay M, Bird A, Reardon W, Guest M, et al. Smith RJ, et al. Among authors: kimberling wj. Genomics. 1992 Dec;14(4):995-1002. doi: 10.1016/s0888-7543(05)80122-3. Genomics. 1992. PMID: 1478678
Connexin 26: required for normal auditory function.
Kelley PM, Cohn E, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Brain Res Brain Res Rev. 2000 Apr;32(1):184-8. doi: 10.1016/s0165-0173(99)00080-6. Brain Res Brain Res Rev. 2000. PMID: 10751669 Review.
New approaches to the treatment of dense deposit disease.
Smith RJ, Alexander J, Barlow PN, Botto M, Cassavant TL, Cook HT, de Córdoba SR, Hageman GS, Jokiranta TS, Kimberling WJ, Lambris JD, Lanning LD, Levidiotis V, Licht C, Lutz HU, Meri S, Pickering MC, Quigg RJ, Rops AL, Salant DJ, Sethi S, Thurman JM, Tully HF, Tully SP, van der Vlag J, Walker PD, Würzner R, Zipfel PF; Dense Deposit Disease Focus Group. Smith RJ, et al. Among authors: kimberling wj. J Am Soc Nephrol. 2007 Sep;18(9):2447-56. doi: 10.1681/ASN.2007030356. Epub 2007 Aug 5. J Am Soc Nephrol. 2007. PMID: 17675665 Free PMC article. Review.
233 results