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

Year Number of Results
1995 3
1996 3
1997 4
1999 3
2000 1
2001 1
2002 2
2003 1
2004 1
2005 2
2006 1
2010 2
2012 1
2024 0

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PubMed (cited) for id: 600856

25 results

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Page 1
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome.
Arboleda VA, Lee H, Parnaik R, Fleming A, Banerjee A, Ferraz-de-Souza B, Délot EC, Rodriguez-Fernandez IA, Braslavsky D, Bergadá I, Dell'Angelica EC, Nelson SF, Martinez-Agosto JA, Achermann JC, Vilain E. Arboleda VA, et al. Nat Genet. 2012 May 27;44(7):788-92. doi: 10.1038/ng.2275. Nat Genet. 2012. PMID: 22634751 Free PMC article.
CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms.
Romanelli V, Belinchón A, Benito-Sanz S, Martínez-Glez V, Gracia-Bouthelier R, Heath KE, Campos-Barros A, García-Miñaur S, Fernandez L, Meneses H, López-Siguero JP, Guillén-Navarro E, Gómez-Puertas P, Wesselink JJ, Mercado G, Esteban-Marfil V, Palomo R, Mena R, Sánchez A, Del Campo M, Lapunzina P. Romanelli V, et al. Am J Med Genet A. 2010 Jun;152A(6):1390-7. doi: 10.1002/ajmg.a.33453. Am J Med Genet A. 2010. PMID: 20503313 Review.
Gene expression patterns in human placenta.
Sood R, Zehnder JL, Druzin ML, Brown PO. Sood R, et al. Proc Natl Acad Sci U S A. 2006 Apr 4;103(14):5478-83. doi: 10.1073/pnas.0508035103. Epub 2006 Mar 27. Proc Natl Acad Sci U S A. 2006. PMID: 16567644 Free PMC article.
25 results