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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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1996 | 1 |
2007 | 1 |
2008 | 1 |
2011 | 2 |
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2015 | 1 |
2024 | 0 |
PubMed (RefSeq) for id: 1958747106
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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.
Eur J Hum Genet. 2015 Sep;23(9):1176-85. doi: 10.1038/ejhg.2014.253. Epub 2014 Nov 26.
Eur J Hum Genet. 2015.
PMID: 25424714
Free PMC article.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD.
Gaudet P, et al.
Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
Brief Bioinform. 2011.
PMID: 21873635
Free PMC article.
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Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.
Sirmaci A, Spiliopoulos M, Brancati F, Powell E, Duman D, Abrams A, Bademci G, Agolini E, Guo S, Konuk B, Kavaz A, Blanton S, Digilio MC, Dallapiccola B, Young J, Zuchner S, Tekin M.
Sirmaci A, et al.
Am J Hum Genet. 2011 Aug 12;89(2):289-94. doi: 10.1016/j.ajhg.2011.06.007. Epub 2011 Jul 21.
Am J Hum Genet. 2011.
PMID: 21782149
Free PMC article.
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An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
Barbaric I, Perry MJ, Dear TN, Rodrigues Da Costa A, Salopek D, Marusic A, Hough T, Wells S, Hunter AJ, Cheeseman M, Brown SD.
Barbaric I, et al.
Physiol Genomics. 2008 Feb 19;32(3):311-21. doi: 10.1152/physiolgenomics.00116.2007. Epub 2007 Nov 6.
Physiol Genomics. 2008.
PMID: 17986521
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Normalization and subtraction: two approaches to facilitate gene discovery.
Bonaldo MF, Lennon G, Soares MB.
Bonaldo MF, et al.
Genome Res. 1996 Sep;6(9):791-806. doi: 10.1101/gr.6.9.791.
Genome Res. 1996.
PMID: 8889548
Free article.
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