Bissler, J J <br/><br/>
Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema.  [electronic resource] 

 -  Human genetics  Mar 1994 
 - 265-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00212020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Angioedema--classification<br/>Base Composition<br/>Base Sequence<br/>Complement C1 Inactivator Proteins--genetics<br/>Consensus Sequence<br/>DNA<br/>Exons<br/>Humans<br/>Models, Genetic<br/>Molecular Sequence Data<br/>Multigene Family<br/>Mutagenesis, Insertional<br/>Nucleic Acid Conformation<br/>Polymerase Chain Reaction<br/>Repetitive Sequences, Nucleic Acid<br/>Sequence Deletion