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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2008 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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Clinical review of genetic epileptic encephalopathies.
Eur J Med Genet. 2012 May;55(5):281-98. doi: 10.1016/j.ejmg.2011.12.010. Epub 2012 Jan 25.
Eur J Med Genet. 2012.
PMID: 22342633
Free PMC article.
Review.
FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence.
Krejci P, Prochazkova J, Smutny J, Chlebova K, Lin P, Aklian A, Bryja V, Kozubik A, Wilcox WR.
Krejci P, et al.
Bone. 2010 Jul;47(1):102-10. doi: 10.1016/j.bone.2010.03.021. Epub 2010 Mar 31.
Bone. 2010.
PMID: 20362703
Free PMC article.
Item in Clipboard
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25.
Burkardt DD, Rosenfeld JA, Helgeson ML, Angle B, Banks V, Smith WE, Gripp KW, Moline J, Moran RT, Niyazov DM, Stevens CA, Zackai E, Lebel RR, Ashley DG, Kramer N, Lachman RS, Graham JM Jr.
Burkardt DD, et al.
Am J Med Genet A. 2011 Jun;155A(6):1336-51. doi: 10.1002/ajmg.a.34049. Epub 2011 May 5.
Am J Med Genet A. 2011.
PMID: 21548129
Free PMC article.
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Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 gene.
Graham JM Jr, Visootsak J, Dykens E, Huddleston L, Clark RD, Jones KL, Moeschler JB, Opitz JM, Morford J, Simensen R, Rogers RC, Schwartz CE, Friez MJ, Stevenson RE.
Graham JM Jr, et al.
Am J Med Genet A. 2008 Dec 1;146A(23):3011-7. doi: 10.1002/ajmg.a.32553.
Am J Med Genet A. 2008.
PMID: 18973276
Free PMC article.
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