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  • 検索条件 : 絞込み (MeSH = Craniofacial Abnormalities / genetics*)
生物種 リソース名 タイトル
ゼブラフィッシュ Tol-056 De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism.
メダカ ESCO2^R80S (MT924) , WS338 , WS339 , TILLING_MUTANT Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes).