Kurahashi, H <br/><br/>
Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.  [electronic resource] 

 -  Human genetics  Mar 1994 
 - 248-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00212017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Blotting, Southern<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 22<br/>Cloning, Molecular<br/>Cosmids<br/>Cricetinae<br/>DiGeorge Syndrome--genetics<br/>Gene Library<br/>Genetic Markers<br/>Heterozygote<br/>Humans<br/>Hybrid Cells<br/>Polymorphism, Restriction Fragment Length<br/>Repetitive Sequences, Nucleic Acid