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

Year Number of Results
1981 1
1987 1
1988 2
1989 1
1990 5
1991 2
1992 1
1996 2
1998 1
2000 1
2002 4
2003 2
2004 5
2005 7
2006 9
2007 13
2008 9
2009 6
2010 5
2011 16
2012 12
2013 7
2014 10
2015 25
2016 23
2017 15
2018 16
2019 19
2020 15
2021 10
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Article attribute
Article type
Publication date

Search Results

215 results
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Page 1
Imprinting disorders in humans: a review.
Butler MG. Butler MG. Curr Opin Pediatr. 2020 Dec;32(6):719-729. doi: 10.1097/MOP.0000000000000965. Curr Opin Pediatr. 2020. PMID: 33148967 Review.
Rare FMR1 gene mutations causing fragile X syndrome: A review.
Sitzmann AF, Hagelstrom RT, Tassone F, Hagerman RJ, Butler MG. Sitzmann AF, et al. Among authors: butler mg. Am J Med Genet A. 2018 Jan;176(1):11-18. doi: 10.1002/ajmg.a.38504. Epub 2017 Nov 27. Am J Med Genet A. 2018. PMID: 29178241 Free PMC article. Review.
The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Cox DM, Butler MG. Cox DM, et al. Among authors: butler mg. Int J Mol Sci. 2015 Feb 13;16(2):4068-82. doi: 10.3390/ijms16024068. Int J Mol Sci. 2015. PMID: 25689425 Free PMC article. Review.
GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.
Deal CL, Tony M, Höybye C, Allen DB, Tauber M, Christiansen JS; 2011 Growth Hormone in Prader-Willi Syndrome Clinical Care Guidelines Workshop Participants. Deal CL, et al. J Clin Endocrinol Metab. 2013 Jun;98(6):E1072-87. doi: 10.1210/jc.2012-3888. Epub 2013 Mar 29. J Clin Endocrinol Metab. 2013. PMID: 23543664 Free PMC article. Review.
215 results
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