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

Year Number of Results
1983 3
1984 3
1985 3
1986 3
1987 2
1988 3
1989 2
1990 3
1991 2
1992 3
1993 3
1994 2
1995 1
1996 1
1997 4
1998 2
1999 2
2000 1
2002 2
2003 3
2004 1
2005 4
2006 1
2007 2
2008 4
2009 3
2010 3
2011 2
2012 5
2013 5
2014 3
2015 2
2016 3
2024 0

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82 results

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Page 1
Noonan syndrome.
Roberts AE, Allanson JE, Tartaglia M, Gelb BD. Roberts AE, et al. Among authors: allanson je. Lancet. 2013 Jan 26;381(9863):333-42. doi: 10.1016/S0140-6736(12)61023-X. Epub 2013 Jan 10. Lancet. 2013. PMID: 23312968 Free PMC article. Review.
Noonan syndrome: clinical features, diagnosis, and management guidelines.
Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Romano AA, et al. Among authors: allanson je. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. Pediatrics. 2010. PMID: 20876176 Review.
Noonan syndrome.
Allanson JE. Allanson JE. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):274-9. doi: 10.1002/ajmg.c.30138. Am J Med Genet C Semin Med Genet. 2007. PMID: 17639592 Review.
Noonan syndrome.
Allanson JE. Allanson JE. J Med Genet. 1987 Jan;24(1):9-13. doi: 10.1136/jmg.24.1.9. J Med Genet. 1987. PMID: 3543368 Free PMC article. Review. No abstract available.
Elements of morphology: introduction.
Allanson JE, Biesecker LG, Carey JC, Hennekam RC. Allanson JE, et al. Am J Med Genet A. 2009 Jan;149A(1):2-5. doi: 10.1002/ajmg.a.32601. Am J Med Genet A. 2009. PMID: 19127575 Free PMC article.
Hemochromatosis.
Allanson JE. Allanson JE. Ariz Med. 1984 Apr;41(4):226-8. Ariz Med. 1984. PMID: 6743031 No abstract available.
Special Section. Syndrome-specific growth charts.
Hall JG, Allanson JE, Gripp KW, Slavotinek AM. Hall JG, et al. Among authors: allanson je. Am J Med Genet A. 2012 Nov;158A(11):2645-6. doi: 10.1002/ajmg.a.35704. Epub 2012 Oct 4. Am J Med Genet A. 2012. PMID: 23038170 No abstract available.
Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.
Peddibhotla S, Nagamani SC, Erez A, Hunter JV, Holder JL Jr, Carlin ME, Bader PI, Perras HM, Allanson JE, Newman L, Simpson G, Immken L, Powell E, Mohanty A, Kang SH, Stankiewicz P, Bacino CA, Bi W, Patel A, Cheung SW. Peddibhotla S, et al. Among authors: allanson je. Eur J Hum Genet. 2015 Jan;23(1):54-60. doi: 10.1038/ejhg.2014.51. Epub 2014 Apr 16. Eur J Hum Genet. 2015. PMID: 24736736 Free PMC article. Review.
82 results