Download Werner Syndrome Chromosome 8 PNG. Chromosome 8 likely contains about 700 genes that provide instructions for making proteins. Werner syndrome (wrn) is an inherited disorder that produces symptoms of premature aging.
It should not to be confused with similarly sounding wermer syndrome.
Men2 syndrome nf1 syndrome rcc renal oncocytoma. It is the result of a translocation between chromosome 9 and 22. A combined syndrome of juvenile polyposis and hereditary hemorrhagic telangiectasia assosiated with mutations madh4 (smad4). Werner syndrome may also be characterized by development of a distinctive high pitched voice;