Berry, Fred B <br/><br/>
The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.  [electronic resource] 

 -  Human molecular genetics  Sep 2005 
 - 2619-27 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddi295  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>DNA Primers<br/>Electrophoretic Mobility Shift Assay<br/>Eyelashes--abnormalities<br/>Fluorescent Antibody Technique<br/>Forkhead Transcription Factors--genetics<br/>Humans<br/>Luciferases<br/>Lymphedema--complications<br/>Models, Genetic<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Mutation, Missense--genetics<br/>Sequence Analysis, DNA