Genetic Analyses Identified a SALL4 Gene Mutation Associated with Holt-Oram Syndrome
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Holt-Oram syndrome (HOS) is an autosomal dominant disorder, which is characterized by deformities of upper limbs and congenital heart defects. Alterations of TBX5 gene have been identified to be the leading cause of HOS, while some cases could not be explained... ...
