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

Year Number of Results
1970 1
1973 1
1975 1
1979 1
1981 1
1982 2
1983 5
1984 3
1986 3
1987 4
1988 5
1989 3
1990 1
1991 6
1992 3
1993 4
1994 1
1995 6
1996 2
1997 7
1998 3
1999 12
2000 6
2001 12
2002 8
2003 10
2004 3
2005 4
2006 4
2007 3
2008 2
2010 3
2011 3
2012 4
2013 3
2014 2
2016 2
2017 1
2020 1
2021 2
2024 0

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144 results

Results by year

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Page 1
Barth syndrome.
Clarke SL, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG. Clarke SL, et al. Among authors: kelley ri. Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23. Orphanet J Rare Dis. 2013. PMID: 23398819 Free PMC article. Review.
The Smith-Lemli-Opitz syndrome.
Kelley RI, Hennekam RC. Kelley RI, et al. J Med Genet. 2000 May;37(5):321-35. doi: 10.1136/jmg.37.5.321. J Med Genet. 2000. PMID: 10807690 Free PMC article. Review.
Inborn errors of sterol biosynthesis.
Kelley RI, Herman GE. Kelley RI, et al. Annu Rev Genomics Hum Genet. 2001;2:299-341. doi: 10.1146/annurev.genom.2.1.299. Annu Rev Genomics Hum Genet. 2001. PMID: 11701653 Review.
Mendelian etiologies of stroke.
Natowicz M, Kelley RI. Natowicz M, et al. Among authors: kelley ri. Ann Neurol. 1987 Aug;22(2):175-92. doi: 10.1002/ana.410220202. Ann Neurol. 1987. PMID: 3310853 Review.
Clinical variability in Rett syndrome.
Naidu S, Bibat G, Kratz L, Kelley RI, Pevsner J, Hoffman E, Cuffari C, Rohde C, Blue ME, Johnston MV. Naidu S, et al. Among authors: kelley ri. J Child Neurol. 2003 Oct;18(10):662-8. doi: 10.1177/08830738030180100801. J Child Neurol. 2003. PMID: 14649546 Review.
Behavioral phenotype of RSH/Smith-Lemli-Opitz syndrome.
Tierney E, Nwokoro NA, Kelley RI. Tierney E, et al. Among authors: kelley ri. Ment Retard Dev Disabil Res Rev. 2000;6(2):131-4. doi: 10.1002/1098-2779(2000)6:2<131::AID-MRDD7>3.0.CO;2-R. Ment Retard Dev Disabil Res Rev. 2000. PMID: 10899806 Review.
A new face for an old syndrome.
Kelley RI. Kelley RI. Am J Med Genet. 1997 Jan 31;68(3):251-6. doi: 10.1002/(sici)1096-8628(19970131)68:3<251::aid-ajmg1>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9024554 No abstract available.
Inherited disorders of cholesterol biosynthesis.
Haas D, Kelley RI, Hoffmann GF. Haas D, et al. Among authors: kelley ri. Neuropediatrics. 2001 Jun;32(3):113-22. doi: 10.1055/s-2001-16618. Neuropediatrics. 2001. PMID: 11521206 Review.
144 results