Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p

This report demonstrates the utility of genomic arrays as a diagnostic tool to better characterize atypical deletions in known syndromes such as 5p– syndrome, which will allow a better understanding of the genotype-phenotype correlations.Mol Syndromol
Source: Molecular Syndromology - Category: Molecular Biology Source Type: research