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

Year Number of Results
1971 2
1972 1
1973 2
1974 2
1993 1
1994 4
1995 5
1996 5
1997 6
1998 1
1999 2
2000 1
2001 1
2002 1
2003 1
2005 1
2006 2
2007 2
2008 1
2009 1
2011 1
2012 1
2013 2
2021 0
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46 results
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Page 1
Aminoglycoside suppression of nonsense mutations in severe hemophilia.
James PD, Raut S, Rivard GE, Poon MC, Warner M, McKenna S, Leggo J, Lillicrap D. James PD, et al. Among authors: leggo j. Blood. 2005 Nov 1;106(9):3043-8. doi: 10.1182/blood-2005-03-1307. Epub 2005 Jul 28. Blood. 2005. PMID: 16051741 Free article.
Different clinical phenotype in triplets with haemophilia A.
Barnes C, Blanchette V, Lillicrap D, Mann K, Stain AM, Leggo J, Hilliard P, Carcao M. Barnes C, et al. Among authors: leggo j. Haemophilia. 2007 Mar;13(2):202-5. doi: 10.1111/j.1365-2516.2006.01396.x. Haemophilia. 2007. PMID: 17286775
B37 repeats are normal in most schizophrenic patients.
Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA, Ross CA, Li SH, Lofthouse R, Crow TJ, DeLisi LE. Rubinsztein DC, et al. Among authors: leggo j. Br J Psychiatry. 1994 Jun;164(6):851-2. doi: 10.1192/bjp.164.6.851. Br J Psychiatry. 1994. PMID: 7953005 No abstract available.
Site of (CCG) polymorphism in the HD gene.
Rubinsztein DC, Leggo J, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Nat Genet. 1993 Nov;5(3):214-5. doi: 10.1038/ng1193-214. Nat Genet. 1993. PMID: 8275082 No abstract available.
46 results
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