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

Year Number of Results
1982 1
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1993 1
1994 3
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1996 2
1998 2
1999 3
2000 2
2001 4
2002 5
2003 3
2004 10
2005 10
2006 10
2007 16
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2011 6
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2017 2
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Similar articles for PMID: 15805155

122 results

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Page 1
Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.
Kleefstra T, Smidt M, Banning MJ, Oudakker AR, Van Esch H, de Brouwer AP, Nillesen W, Sistermans EA, Hamel BC, de Bruijn D, Fryns JP, Yntema HG, Brunner HG, de Vries BB, van Bokhoven H. Kleefstra T, et al. J Med Genet. 2005 Apr;42(4):299-306. doi: 10.1136/jmg.2004.028464. J Med Genet. 2005. PMID: 15805155 Free PMC article.
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
Kleefstra T, van Zelst-Stams WA, Nillesen WM, Cormier-Daire V, Houge G, Foulds N, van Dooren M, Willemsen MH, Pfundt R, Turner A, Wilson M, McGaughran J, Rauch A, Zenker M, Adam MP, Innes M, Davies C, López AG, Casalone R, Weber A, Brueton LA, Navarro AD, Bralo MP, Venselaar H, Stegmann SP, Yntema HG, van Bokhoven H, Brunner HG. Kleefstra T, et al. J Med Genet. 2009 Sep;46(9):598-606. doi: 10.1136/jmg.2008.062950. Epub 2009 Mar 4. J Med Genet. 2009. PMID: 19264732 Free article.
The chromosome 9q subtelomere deletion syndrome.
Stewart DR, Kleefstra T. Stewart DR, et al. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):383-92. doi: 10.1002/ajmg.c.30148. Am J Med Genet C Semin Med Genet. 2007. PMID: 17910072 Review.
122 results