Tassabehji, M <br/><br/>
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse.  [electronic resource] 

 -  Human molecular genetics  Jul 1994 
 - 1069-74 p.  digital 
<br/><br/> Publication Type: Case Reports; 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/3.7.1069  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Cell Movement<br/>Chromosomes, Human, Pair 2<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Exons<br/>Genes<br/>Genes, Homeobox<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mice<br/>Mice, Mutant Strains--genetics<br/>Molecular Sequence Data<br/>Neural Crest--pathology<br/>PAX3 Transcription Factor<br/>Paired Box Transcription Factors<br/>Phenotype<br/>Point Mutation<br/>RNA Splicing<br/>Sequence Deletion<br/>Species Specificity<br/>Transcription Factors<br/>Waardenburg Syndrome--genetics