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

Year Number of Results
1947 1
1973 1
1978 1
1979 1
1980 1
1981 5
1982 3
1983 5
1984 2
1985 4
1986 7
1987 23
1988 14
1989 9
1990 13
1991 12
1992 9
1993 11
1994 5
1995 10
1996 12
1997 9
1998 14
1999 10
2000 12
2001 4
2002 8
2003 5
2004 6
2005 10
2006 13
2007 16
2008 13
2009 9
2010 6
2011 22
2012 21
2013 11
2014 20
2015 37
2016 32
2017 24
2018 24
2019 23
2020 16
2021 14
2022 22
2023 13
2024 2

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512 results

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Page 1
Special Issue: Genetics of Prader-Willi Syndrome.
Godler DE, Butler MG. Godler DE, et al. Among authors: butler mg. Genes (Basel). 2021 Sep 16;12(9):1429. doi: 10.3390/genes12091429. Genes (Basel). 2021. PMID: 34573411 Free PMC article.
Genetics of Obesity in Humans: A Clinical Review.
Mahmoud R, Kimonis V, Butler MG. Mahmoud R, et al. Among authors: butler mg. Int J Mol Sci. 2022 Sep 20;23(19):11005. doi: 10.3390/ijms231911005. Int J Mol Sci. 2022. PMID: 36232301 Free PMC article. Review.
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 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.
Clinical Trials in Prader-Willi Syndrome: A Review.
Mahmoud R, Kimonis V, Butler MG. Mahmoud R, et al. Among authors: butler mg. Int J Mol Sci. 2023 Jan 21;24(3):2150. doi: 10.3390/ijms24032150. Int J Mol Sci. 2023. PMID: 36768472 Free PMC article. 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.
512 results