Clifton-Bligh, R J <br/><br/>
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia.  [electronic resource] 

 -  Nature genetics  Aug 1998 
 - 399-401 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/1294  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Amino Acid Sequence<br/>Cell Line<br/>Choanal Atresia--genetics<br/>Cleft Palate--genetics<br/>DNA--metabolism<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Fibroblasts<br/>Forkhead Transcription Factors<br/>Genes, Regulator--physiology<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Organ Specificity<br/>Point Mutation--genetics<br/>Protein Binding<br/>RNA, Messenger--analysis<br/>Repressor Proteins--genetics<br/>Sequence Homology, Amino Acid<br/>Testis--chemistry<br/>Thyroid Gland--abnormalities<br/>Transcription Factors--genetics