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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1999 | 1 |
2000 | 1 |
2015 | 1 |
2017 | 1 |
2018 | 3 |
2024 | 0 |
PubMed (OMIM) for id: 10785
6 results
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Page 1
Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.
Am J Med Genet A. 2018 Nov;176(11):2460-2465. doi: 10.1002/ajmg.a.40489. Epub 2018 Aug 6.
Am J Med Genet A. 2018.
PMID: 30079490
Free PMC article.
Speech and language delay in a patient with WDR4 mutations.
Chen X, Gao Y, Yang L, Wu B, Dong X, Liu B, Lu Y, Zhou W, Wang H.
Chen X, et al.
Eur J Med Genet. 2018 Aug;61(8):468-472. doi: 10.1016/j.ejmg.2018.03.007. Epub 2018 Mar 26.
Eur J Med Genet. 2018.
PMID: 29597095
Item in Clipboard
Further delineation of the phenotype caused by biallelic variants in the WDR4 gene.
Trimouille A, Lasseaux E, Barat P, Deiller C, Drunat S, Rooryck C, Arveiler B, Lacombe D.
Trimouille A, et al.
Clin Genet. 2018 Feb;93(2):374-377. doi: 10.1111/cge.13074. Epub 2017 Sep 29.
Clin Genet. 2018.
PMID: 28617965
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Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfism.
Shaheen R, Abdel-Salam GM, Guy MP, Alomar R, Abdel-Hamid MS, Afifi HH, Ismail SI, Emam BA, Phizicky EM, Alkuraya FS.
Shaheen R, et al.
Genome Biol. 2015 Sep 28;16:210. doi: 10.1186/s13059-015-0779-x.
Genome Biol. 2015.
PMID: 26416026
Free PMC article.
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Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein.
Michaud J, Kudoh J, Berry A, Bonne-Tamir B, Lalioti MD, Rossier C, Shibuya K, Kawasaki K, Asakawa S, Minoshima S, Shimizu N, Antonarakis SE, Scott HS.
Michaud J, et al.
Genomics. 2000 Aug 15;68(1):71-9. doi: 10.1006/geno.2000.6258.
Genomics. 2000.
PMID: 10950928
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Cloning and expression analysis of a novel WD repeat gene, WDR3, mapping to 1p12-p13.
Claudio JO, Liew CC, Ma J, Heng HH, Stewart AK, Hawley RG.
Claudio JO, et al.
Genomics. 1999 Jul 1;59(1):85-9. doi: 10.1006/geno.1999.5858.
Genomics. 1999.
PMID: 10395803
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