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

Year Number of Results
1949 1
1967 1
1978 1
1982 1
1983 3
1984 3
1985 3
1986 4
1987 4
1988 4
1989 8
1990 3
1991 4
1992 6
1993 5
1994 4
1995 1
1996 2
1997 8
1998 4
1999 4
2000 2
2001 3
2002 6
2003 6
2004 4
2005 5
2006 3
2007 5
2008 10
2009 26
2010 9
2011 5
2012 17
2013 12
2014 10
2015 9
2016 6
2017 1
2018 5
2019 4
2020 2
2021 2
Text availability
Article attribute
Article type
Publication date

Search Results

210 results
Results by year
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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, Roberts AE. Allanson JE, et al. 2001 Nov 15 [updated 2019 Aug 8]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 2001 Nov 15 [updated 2019 Aug 8]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 20301303 Free Books & Documents. Review.
Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases.
Verloes A, Di Donato N, Masliah-Planchon J, Jongmans M, Abdul-Raman OA, Albrecht B, Allanson J, Brunner H, Bertola D, Chassaing N, David A, Devriendt K, Eftekhari P, Drouin-Garraud V, Faravelli F, Faivre L, Giuliano F, Guion Almeida L, Juncos J, Kempers M, Eker HK, Lacombe D, Lin A, Mancini G, Melis D, Lourenço CM, Siu VM, Morin G, Nezarati M, Nowaczyk MJ, Ramer JC, Osimani S, Philip N, Pierpont ME, Procaccio V, Roseli ZS, Rossi M, Rusu C, Sznajer Y, Templin L, Uliana V, Klaus M, Van Bon B, Van Ravenswaaij C, Wainer B, Fry AE, Rump A, Hoischen A, Drunat S, Rivière JB, Dobyns WB, Pilz DT. Verloes A, et al. Among authors: allanson j. Eur J Hum Genet. 2015 Mar;23(3):292-301. doi: 10.1038/ejhg.2014.95. Epub 2014 Jul 23. Eur J Hum Genet. 2015. PMID: 25052316 Free PMC article.
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.
The cardiofaciocutaneous syndrome.
Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. Roberts A, et al. Among authors: allanson j. J Med Genet. 2006 Nov;43(11):833-42. doi: 10.1136/jmg.2006.042796. Epub 2006 Jul 6. J Med Genet. 2006. PMID: 16825433 Free PMC article. Review.
Hemochromatosis.
Allanson JE. Allanson JE. Ariz Med. 1984 Apr;41(4):226-8. Ariz Med. 1984. PMID: 6743031 No abstract available.
Genetics: schizophrenia.
Rideout AL, Carroll JC, Blaine SM, Cremin C, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Allanson J. Rideout AL, et al. Among authors: allanson j. Can Fam Physician. 2009 Dec;55(12):1207. Can Fam Physician. 2009. PMID: 20008600 Free PMC article. No abstract available.
210 results
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