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Results by year

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

Year Number of Results
1959 1
1961 1
1966 2
1968 1
1969 1
1972 1
1974 1
1975 2
1976 1
1979 2
1980 3
1981 3
1982 6
1983 4
1984 1
1985 5
1986 3
1987 5
1988 2
1989 6
1991 3
1992 3
1993 4
1994 3
1995 5
1996 10
1997 3
1998 5
1999 3
2000 4
2001 5
2002 2
2003 3
2004 4
2005 5
2006 6
2007 13
2008 8
2009 5
2010 2
2011 3
2012 2
2013 3
2014 2
2015 1
2016 2
2017 4
2018 2
2019 5
2020 2
2021 1
2022 2
2024 0

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Similar articles for PMID: 12439898

168 results

Results by year

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Page 1
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.
Digilio MC, Pacileo G, Sarkozy A, Limongelli G, Conti E, Cerrato F, Marino B, Pizzuti A, Calabrò R, Dallapiccola B. Digilio MC, et al. Birth Defects Res A Clin Mol Teratol. 2004 Feb;70(2):95-8. doi: 10.1002/bdra.10148. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 14991917
Noonan syndrome: the changing phenotype.
Allanson JE, Hall JG, Hughes HE, Preus M, Witt RD. Allanson JE, et al. Am J Med Genet. 1985 Jul;21(3):507-14. doi: 10.1002/ajmg.1320210313. Am J Med Genet. 1985. PMID: 4025385
168 results