Related Articles
A frameshift mutation in the <em>SCNN1B</em> gene in a family with Liddle syndrome: A case report and systematic review
Familial Lynch syndrome with early age of onset and confirmed splice site mutation in MSH2: A case report
Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia
A novel germline mutation of hMLH1 in a Korean hereditary non-polyposis colorectal cancer family
Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome