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

Year Number of Results
1976 1
1981 1
1985 1
1986 1
1987 2
1988 1
1989 3
1990 2
1991 2
1992 2
1993 4
1994 5
1995 2
1996 2
1998 1
1999 2
2001 1
2002 1
2004 1
2006 1
2008 2
2009 1
2010 2
2011 1
2013 1
2014 2
2024 0

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44 results

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Page 1
Smith-Magenis syndrome and tetralogy of Fallot.
Sweeney E, Peart I, Tofeig M, Kerr B. Sweeney E, et al. Among authors: peart i. J Med Genet. 1999 Jun;36(6):501-2. J Med Genet. 1999. PMID: 10874646 Free PMC article. No abstract available.
Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.
Griffin HR, Hall DH, Topf A, Eden J, Stuart AG, Parsons J, Peart I, Deanfield JE, O'Sullivan J, Babu-Narayan SV, Gatzoulis MA, Bu'lock FA, Bhattacharya S, Bentham J, Farrall M, Granados Riveron J, Brook JD, Burn J, Cordell HJ, Goodship JA, Keavney B. Griffin HR, et al. Among authors: peart i. PLoS One. 2009;4(3):e4978. doi: 10.1371/journal.pone.0004978. Epub 2009 Mar 24. PLoS One. 2009. PMID: 19308252 Free PMC article.
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.
Griffin HR, Töpf A, Glen E, Zweier C, Stuart AG, Parsons J, Peart I, Deanfield J, O'Sullivan J, Rauch A, Scambler P, Burn J, Cordell HJ, Keavney B, Goodship JA. Griffin HR, et al. Among authors: peart i. Heart. 2010 Oct;96(20):1651-5. doi: 10.1136/hrt.2010.200121. Heart. 2010. PMID: 20937753 Free PMC article.
44 results