Hargrave, M <br/><br/>
Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases.  [electronic resource] 

 -  Human genetics  Apr 2000 
 - 432-9 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>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390000266  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Blepharophimosis--genetics<br/>Blepharoptosis--genetics<br/>Charcot-Marie-Tooth Disease--genetics<br/>Chick Embryo<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3<br/>Eye Abnormalities--genetics<br/>Genetic Testing<br/>High Mobility Group Proteins--genetics<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Mice<br/>Mobius Syndrome--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>SOXB2 Transcription Factors<br/>Sequence Homology, Amino Acid