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  • 検索条件 : 絞込み (MeSH = Developmental Disabilities / genetics*)
生物種 リソース名 タイトル
ショウジョウバエ DGRC#205260 TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
ゼブラフィッシュ Tol-056 De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism.
ゼブラフィッシュ Tg(EF1α:mKO2-zCdt1(1/190)) , Tg(EF1α:mAG-hGem(1/60)) Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control.