Biancalana, V <br/><br/>
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.  [electronic resource] 

 -  American journal of human genetics  May 1992 
 - 981-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Female<br/>Genetic Linkage--genetics<br/>Genetic Markers--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Polymorphism, Restriction Fragment Length<br/>Syndrome<br/>X Chromosome