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Details Of Syndromic Child Disease

Disease Name phenotype Inheritance Mode Chr Location Mutation Type Gene Name mRNA Variant Protein Variant Effect Reference
Laurin-Sandrow syndrome, Haas-type polysyndactyly polysyndactyly,mirror image duplication, etc Autosomal Dominant 7q36 Duplication 47kbDup Lohan et al., 2014/2014