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Results by year

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

Year Number of Results
1975 1
1978 1
1979 1
1981 1
1984 4
1986 2
1987 3
1988 1
1989 2
1990 2
1991 3
1992 5
1993 7
1994 5
1995 6
1996 8
1997 8
1998 8
1999 10
2000 5
2001 11
2002 2
2003 9
2004 7
2005 10
2006 12
2007 9
2008 7
2009 6
2010 9
2011 10
2012 12
2013 7
2014 11
2015 13
2016 7
2017 11
2018 16
2019 9
2020 21
2021 16
2022 14
2023 14
2024 1

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PubMed for id: 870948

295 results

Results by year

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Page 1
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele.
Crane-Smith Z, De Castro SCP, Nikolopoulou E, Wolujewicz P, Smedley D, Lei Y, Mather E, Santos C, Hopkinson M, Pitsillides AA; Genomics England Research Consortium; Finnell RH, Ross ME, Copp AJ, Greene NDE. Crane-Smith Z, et al. Hum Mol Genet. 2023 Aug 26;32(17):2681-2692. doi: 10.1093/hmg/ddad094. Hum Mol Genet. 2023. PMID: 37364051 Free PMC article.
Börjeson-Forssman-Lehmann syndrome: A case report.
Pan L, Yin F, Chen S, Xiong J, He F, Peng J. Pan L, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Feb 28;48(2):294-301. doi: 10.11817/j.issn.1672-7347.2023.220414. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 36999477 Free article. Chinese, English.
295 results