[Clinical characteristics and genetic analysis of three fetuses with Baraitser-Winter cerebrofrontofacial syndrome and Dystonia-deafness syndrome type 1 due to variants of ACTB gene]
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Objective: To study the clinical and genetic characteristics of three fetuses with Baraitser-Winter cerebrofrontofacial syndrome (BWCFF) and Dystonia-deafness syndrome type 1 (DDS1) due to variants of the β-actin (ACTB) gene. ... ...
