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TITLE: SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome  Full Text
AUTHORS: Chiara Migliore; Anna Vendramin; Shane McKee; Paolo Prontera; Francesca Faravelli; Rani Sachdev; Patricia Dias; Martina Mascaro; Danilo Licastro; Germana Meroni;
PUBLISHED: 2022, SOURCE: Genes, VOLUME: 13, ISSUE: 2
INDEXED IN: Scopus