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Year | Number of Results |
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2001 | 1 |
2002 | 1 |
2014 | 1 |
2015 | 1 |
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PubMed (cited) for id: 615049
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WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome.
J Med Genet. 2015 Nov;52(11):754-61. doi: 10.1136/jmedgenet-2015-103069. Epub 2015 Aug 11.
J Med Genet. 2015.
PMID: 26264232
De novo mutations in moderate or severe intellectual disability.
Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL.
Hamdan FF, et al.
PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct.
PLoS Genet. 2014.
PMID: 25356899
Free PMC article.
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WAC, a novel WW domain-containing adapter with a coiled-coil region, is colocalized with splicing factor SC35.
Xu GM, Arnaout MA.
Xu GM, et al.
Genomics. 2002 Jan;79(1):87-94. doi: 10.1006/geno.2001.6684.
Genomics. 2002.
PMID: 11827461
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Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O.
Nagase T, et al.
DNA Res. 2001 Apr 27;8(2):85-95. doi: 10.1093/dnares/8.2.85.
DNA Res. 2001.
PMID: 11347906
Free article.
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