Robinson, W P <br/><br/>
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.  [electronic resource] 

 -  Genomics  May 1996 
 - 17-23 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.1996.0237  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 7<br/>Databases, Factual<br/>Elastin--genetics<br/>Female<br/>Genetic Markers<br/>Heterozygote<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic<br/>Repetitive Sequences, Nucleic Acid<br/>Sequence Deletion<br/>Sequence Homology, Nucleic Acid<br/>Williams Syndrome--genetics