Ophoff, R A <br/><br/>
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.  [electronic resource] 

 -  American journal of human genetics  Aug 2001 
 - 447-53 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/321975  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3--genetics<br/>Female<br/>Haplotypes--genetics<br/>Humans<br/>Kidney Diseases--genetics<br/>Lod Score<br/>Male<br/>Microsatellite Repeats--genetics<br/>Middle Aged<br/>Migraine Disorders--complications<br/>Molecular Sequence Data<br/>Netherlands<br/>Pedigree<br/>Penetrance<br/>Raynaud Disease--complications<br/>Retinal Diseases--complications<br/>Stroke--genetics<br/>Vascular Diseases--complications