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Year | Number of Results |
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1997 | 1 |
2005 | 1 |
2016 | 1 |
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PubMed (OMIM) for id: 8326
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A human neurodevelopmental model for Williams syndrome.
Nature. 2016 Aug 18;536(7616):338-43. doi: 10.1038/nature19067. Epub 2016 Aug 10.
Nature. 2016.
PMID: 27509850
Free PMC article.
Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval.
Zhao C, Avilés C, Abel RA, Almli CR, McQuillen P, Pleasure SJ.
Zhao C, et al.
Development. 2005 Jun;132(12):2917-27. doi: 10.1242/dev.01871.
Development. 2005.
PMID: 15930120
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A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23.
Wang YK, Samos CH, Peoples R, Pérez-Jurado LA, Nusse R, Francke U.
Wang YK, et al.
Hum Mol Genet. 1997 Mar;6(3):465-72. doi: 10.1093/hmg/6.3.465.
Hum Mol Genet. 1997.
PMID: 9147651
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