Price, J A <br/><br/>
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome.  [electronic resource] 

 -  Human molecular genetics  Mar 1998 
 - 563-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/7.3.563  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Bone and Bones--abnormalities<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 17<br/>DNA Mutational Analysis<br/>Exons<br/>Genes, Homeobox<br/>Genetic Markers<br/>Hair--abnormalities<br/>Haplotypes<br/>Homeodomain Proteins--chemistry<br/>Humans<br/>Mice<br/>Molecular Sequence Data<br/>Multigene Family<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Syndrome<br/>Tooth Abnormalities--genetics<br/>Transcription Factors--biosynthesis