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

Year Number of Results
1965 1
1966 1
1967 3
1968 2
1969 5
1970 3
1971 3
1972 1
1973 2
1974 2
1975 3
1976 5
1977 3
1978 1
1979 2
1980 3
1983 2
1984 2
1985 5
1986 2
1988 4
1989 1
1990 5
1991 6
1992 8
1993 4
1994 2
1995 2
1996 4
1997 8
1998 9
1999 5
2000 3
2001 7
2002 9
2003 8
2004 5
2005 9
2006 15
2007 6
2008 12
2009 21
2010 25
2011 30
2012 17
2013 22
2014 26
2015 24
2016 17
2017 18
2018 23
2019 28
2020 24
2021 25
2022 18
2023 16
2024 6

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471 results

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Page 1
VACTERL/VATER Association.
Solomon BD. Solomon BD. Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56. Orphanet J Rare Dis. 2011. PMID: 21846383 Free PMC article. Review.
Pediatric Pes Planus: A State-of-the-Art Review.
Carr JB 2nd, Yang S, Lather LA. Carr JB 2nd, et al. Pediatrics. 2016 Mar;137(3):e20151230. doi: 10.1542/peds.2015-1230. Epub 2016 Feb 17. Pediatrics. 2016. PMID: 26908688 Review.
22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E. Goldmuntz E. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):64-72. doi: 10.1002/ajmg.c.31774. Epub 2020 Feb 12. Am J Med Genet C Semin Med Genet. 2020. PMID: 32049433 Review.
Hypothesis: Symbrachydactyly.
Holmes LB, Nasri HZ. Holmes LB, et al. Am J Med Genet A. 2022 Nov;188(11):3236-3241. doi: 10.1002/ajmg.a.62941. Epub 2022 Sep 8. Am J Med Genet A. 2022. PMID: 36073773
Brachydactyly.
Temtamy SA, Aglan MS. Temtamy SA, et al. Orphanet J Rare Dis. 2008 Jun 13;3:15. doi: 10.1186/1750-1172-3-15. Orphanet J Rare Dis. 2008. PMID: 18554391 Free PMC article. Review.
471 results