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Year | Number of Results |
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2003 | 1 |
2005 | 1 |
2006 | 1 |
2013 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 6468
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The novel ubiquitin ligase complex, SCF(Fbxw4), interacts with the COP9 signalosome in an F-box dependent manner, is mutated, lost and under-expressed in human cancers.
PLoS One. 2013 May 2;8(5):e63610. doi: 10.1371/journal.pone.0063610. Print 2013.
PLoS One. 2013.
PMID: 23658844
Free PMC article.
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
Everman DB, Morgan CT, Lyle R, Laughridge ME, Bamshad MJ, Clarkson KB, Colby R, Gurrieri F, Innes AM, Roberson J, Schrander-Stumpel C, van Bokhoven H, Antonarakis SE, Schwartz CE.
Everman DB, et al.
Am J Med Genet A. 2006 Jul 1;140(13):1375-83. doi: 10.1002/ajmg.a.31246.
Am J Med Genet A. 2006.
PMID: 16761290
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Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T.
Kano H, et al.
Hum Genet. 2005 Dec;118(3-4):477-83. doi: 10.1007/s00439-005-0074-0. Epub 2005 Oct 19.
Hum Genet. 2005.
PMID: 16235095
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A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
de Mollerat XJ, Gurrieri F, Morgan CT, Sangiorgi E, Everman DB, Gaspari P, Amiel J, Bamshad MJ, Lyle R, Blouin JL, Allanson JE, Le Marec B, Wilson M, Braverman NE, Radhakrishna U, Delozier-Blanchet C, Abbott A, Elghouzzi V, Antonarakis S, Stevenson RE, Munnich A, Neri G, Schwartz CE.
de Mollerat XJ, et al.
Hum Mol Genet. 2003 Aug 15;12(16):1959-71. doi: 10.1093/hmg/ddg212.
Hum Mol Genet. 2003.
PMID: 12913067
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