Gaudenz, K <br/><br/>
Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4.  [electronic resource] 

 -  Molecular genetics and metabolism  May 1998 
 - 76-9 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>1096-7192 
<br/><br/><label>Standard No.: </label>10.1006/mgme.1998.2694  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acrocephalosyndactylia--genetics<br/>Arginine<br/>Base Sequence<br/>Child<br/>Craniosynostoses--genetics<br/>Deoxyribonucleases, Type II Site-Specific<br/>Genetic Testing<br/>Humans<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Single-Stranded Conformational<br/>Proline<br/>Protein-Tyrosine Kinases<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Receptor, Fibroblast Growth Factor, Type 1<br/>Receptor, Fibroblast Growth Factor, Type 2<br/>Receptor, Fibroblast Growth Factor, Type 3<br/>Receptor, Fibroblast Growth Factor, Type 4<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Sequence Homology, Amino Acid