Diagnostic Genetics at a Distance: Von Hippel-Lindau Disease and a Novel Mutation

<table>Family pedigree. Patients 1 and 2 = New Zealand; patients 3 and 4 = Iraq. The three deaths in the siblings of patient 2 were due to a coincidental autosomal recessive disease (Hurler syndrome). Filled symbol = presumed VHL; shaded symbol = presumed heterozygote (no known overt disease); ? = apparently unaffected, seeking genetic advice.</table>

Genetics Research International

fig1

Figure 1

Figure 1: Diagnostic Genetics at a Distance: Von Hippel-Lindau Disease and a Novel Mutation 