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

Year Number of Results
1966 1
1967 1
1975 1
1980 3
1982 4
1983 1
1985 1
1988 1
1989 1
1990 1
1991 1
1992 2
1993 3
1995 1
1998 1
1999 1
2000 1
2001 1
2003 1
2004 1
2005 2
2007 2
2008 2
2009 1
2010 1
2011 3
2012 2
2013 8
2014 4
2015 2
2016 1
2017 1
2018 1
2019 1
2025 0

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52 results

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Page 1
Health supervision for children with fragile X syndrome.
Hersh JH, Saul RA; Committee on Genetics. Hersh JH, et al. Among authors: saul ra. Pediatrics. 2011 May;127(5):994-1006. doi: 10.1542/peds.2010-3500. Epub 2011 Apr 25. Pediatrics. 2011. PMID: 21518720 Review.
22q13 deletion syndrome.
Phelan MC, Rogers RC, Saul RA, Stapleton GA, Sweet K, McDermid H, Shaw SR, Claytor J, Willis J, Kelly DP. Phelan MC, et al. Among authors: saul ra. Am J Med Genet. 2001 Jun 15;101(2):91-9. doi: 10.1002/1096-8628(20010615)101:2<91::aid-ajmg1340>3.0.co;2-c. Am J Med Genet. 2001. PMID: 11391650
Molecular diagnostic testing.
Saul RA. Saul RA. Genet Med. 2015 Sep;17(9):761. doi: 10.1038/gim.2015.115. Genet Med. 2015. PMID: 26331191 Free article. No abstract available.
Epigenetics and primary care.
Wright R, Saul RA. Wright R, et al. Among authors: saul ra. Pediatrics. 2013 Dec;132(Suppl 3):S216-23. doi: 10.1542/peds.2013-1032F. Pediatrics. 2013. PMID: 24298130 Review.
52 results