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Results by year

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

Year Number of Results
1910 1
1976 1
1977 1
1979 1
1984 2
1986 2
1987 1
1988 1
1989 2
1990 5
1991 4
1992 5
1993 6
1994 6
1995 5
1996 11
1997 13
1998 19
1999 13
2000 16
2001 13
2002 7
2003 10
2004 10
2005 8
2006 9
2007 6
2008 5
2009 11
2010 9
2011 12
2012 7
2013 10
2014 7
2015 10
2016 2
2017 4
2018 6
2019 3
2020 7
2021 8
2022 4
2023 2
2024 0

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Similar articles for PMID: 11134237

275 results

Results by year

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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.
Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: clinical report and review of the literature.
Castronovo C, Crippa M, Bestetti I, Rusconi D, Russo S, Larizza L, Sangermani R, Bonati MT, Finelli P. Castronovo C, et al. Am J Med Genet A. 2015 Jan;167A(1):221-30. doi: 10.1002/ajmg.a.36815. Epub 2014 Oct 22. Am J Med Genet A. 2015. PMID: 25339188 Review.
[Prader-Willi syndrome and genomic imprinting].
Wang W, Wang DF, Cui YF, Ni JH, Dong ZY, Fu MF, Fu HM, Lu GQ, Chen FS. Wang W, et al. Zhonghua Er Ke Za Zhi. 2003 Jun;41(6):453-6. Zhonghua Er Ke Za Zhi. 2003. PMID: 14749005 Chinese.
275 results