Dietz, H C <br/><br/>
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains.  [electronic resource] 

 -  Human mutation  1992 
 - 366-74 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1059-7794 
<br/><br/><label>Standard No.: </label>10.1002/humu.1380010504  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Cysteine--genetics<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Epidermal Growth Factor--genetics<br/>Fibrillin-1<br/>Fibrillins<br/>Humans<br/>Marfan Syndrome--genetics<br/>Microfilament Proteins--chemistry<br/>Molecular Sequence Data<br/>Molecular Structure<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic<br/>Repetitive Sequences, Nucleic Acid