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

Year Number of Results
1978 1
1980 1
1981 3
1986 1
1987 2
1988 2
1989 10
1990 5
1991 8
1992 9
1993 9
1994 4
1995 2
1996 6
1997 1
1998 2
1999 1
2000 2
2001 2
2003 1
2004 1
2006 1
2007 3
2008 2
2009 1
2010 1
2011 2
2012 1
2014 2
2015 1
2016 2
2022 0
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Search Results

88 results
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Page 1
Alport syndrome--clinical phenotypes, incidence, and pathology.
Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL. Gregory MC, et al. Among authors: barker df. Contrib Nephrol. 1996;117:1-28. doi: 10.1159/000424804. Contrib Nephrol. 1996. PMID: 8801040 Review. No abstract available.
Hearing loss.
Gregory MC, Atkins CL, Barker DF. Gregory MC, et al. Among authors: barker df. N Engl J Med. 1994 Mar 10;330(10):714; author reply 715. doi: 10.1056/nejm199403103301014. N Engl J Med. 1994. PMID: 8141909 No abstract available.
A genetic map of human chromosome 17p.
Wright EC, Goldgar DE, Fain PR, Barker DF, Skolnick MH. Wright EC, et al. Among authors: barker df. Genomics. 1990 May;7(1):103-9. doi: 10.1016/0888-7543(90)90524-x. Genomics. 1990. PMID: 2335351
DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Lupski JR, de Oca-Luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ, Saucedo-Cardenas O, Barker DF, Killian JM, Garcia CA, Chakravarti A, Patel PI. Lupski JR, et al. Among authors: barker df. Cell. 1991 Jul 26;66(2):219-32. doi: 10.1016/0092-8674(91)90613-4. Cell. 1991. PMID: 1677316
88 results