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

Year Number of Results
1977 1
1979 3
1980 5
1982 3
1983 6
1984 12
1985 6
1986 3
1987 2
1989 5
1990 4
1991 6
1992 6
1993 6
1994 3
1995 1
1996 5
1997 1
1998 2
1999 1
2000 2
2003 2
2004 3
2005 3
2006 3
2009 1
2010 1
2012 3
2013 5
2014 1
2015 1
2016 2
2017 1
2019 2
2020 1
2021 1
2024 0

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Similar articles for PMID: 6851221

111 results

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Page 1
Translocations in Prader-Willi syndrome.
Charrow J, Balkin N, Cohen MM. Charrow J, et al. Clin Genet. 1983 Apr;23(4):304-7. doi: 10.1111/j.1399-0004.1983.tb01881.x. Clin Genet. 1983. PMID: 6851221
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.
111 results