Van de Vosse, E <br/><br/>
An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.  [electronic resource] 

 -  European journal of human genetics : EJHG  1996 
 - 101-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1159/000472177  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Mapping<br/>Chromosomes, Artificial, Yeast<br/>Darier Disease--genetics<br/>Female<br/>Humans<br/>Hypophosphatemia, Familial--genetics<br/>Male<br/>Pedigree<br/>Retinal Degeneration--genetics<br/>Syndrome<br/>X Chromosome