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

Year Number of Results
1963 1
1983 1
1985 1
1986 1
1987 6
1988 6
1989 3
1990 1
1991 3
1992 3
1993 6
1994 3
1995 3
1996 6
1997 7
1998 6
1999 5
2000 7
2001 2
2002 4
2003 7
2004 5
2005 6
2006 7
2007 10
2008 7
2009 9
2010 6
2011 2
2012 10
2013 3
2014 8
2015 4
2016 6
2017 6
2018 8
2019 6
2020 4
2021 4
2022 2
2024 0

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Similar articles for PMID: 10323734

181 results

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Page 1
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome.
Cormier-Daire V, Le Merrer M, Gigarel N, Morichon N, Prieur M, Lyonnet S, Vekemans M, Munnich A. Cormier-Daire V, et al. Am J Med Genet. 1997 Mar 17;69(2):166-8. doi: 10.1002/(sici)1096-8628(19970317)69:2<166::aid-ajmg9>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9056554
Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
Polityko AD, Goncharova E, Shamgina L, Drozdovskaja N, Podleschuk L, Abramchik E, Jaroshevich E, Khurs O, Pisarik I, Pribushenya O, Rumyantseva N, Naumchik I. Polityko AD, et al. J Histochem Cytochem. 2005 Mar;53(3):361-4. doi: 10.1369/jhc.4A6402.2005. J Histochem Cytochem. 2005. PMID: 15750020
Pallister-Killian syndrome: report of one case.
Wu HC, Lin LH, Tsai LP, Huang CH, Hung KL, Liao HT. Wu HC, et al. Acta Paediatr Taiwan. 2006 May-Jun;47(3):139-41. Acta Paediatr Taiwan. 2006. PMID: 17078467
181 results