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

Year Number of Results
1983 1
1987 3
1988 1
1989 1
1991 2
1992 3
1993 1
1994 2
1995 3
1996 9
1997 4
1998 3
1999 6
2000 5
2001 3
2003 6
2004 3
2005 6
2006 3
2007 4
2008 5
2009 1
2010 3
2011 3
2012 2
2013 3
2014 4
2015 1
2016 3
2018 2
2019 3
2020 2
2021 2
2022 1
2023 1
2024 0

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Similar articles for PMID: 20082457

101 results

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Page 1
Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.
Chen CP, Lin MH, Chen YY, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Lee MS, Pan CW, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2021 Mar;60(2):335-340. doi: 10.1016/j.tjog.2021.01.012. Taiwan J Obstet Gynecol. 2021. PMID: 33678338 Free article.
Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature.
Xefteris A, Sekerli E, Arampatzi A, Charisiou S, Oikonomidou E, Efstathiou G, Peroulis N, Malamidou A, Tsoulou-Panidou E, Agakidou E, Sarafidis K, Psarakis A, Kataras T, Daskalakis G. Xefteris A, et al. Cytogenet Genome Res. 2019;159(3):109-118. doi: 10.1159/000504159. Epub 2019 Dec 10. Cytogenet Genome Res. 2019. PMID: 31816617 Review.
101 results