Brown, M R <br/><br/>
Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene.  [electronic resource] 

 -  Hormone research  1998 
 - 98-102 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0301-0163 
<br/><br/><label>Standard No.: </label>10.1159/000023134  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>DNA-Binding Proteins--genetics<br/>Exons<br/>Growth Hormone--therapeutic use<br/>Heterozygote<br/>Humans<br/>Hypothyroidism--genetics<br/>Infant<br/>Male<br/>Mutation--physiology<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Thyroxine--therapeutic use<br/>Transcription Factor Pit-1<br/>Transcription Factors--genetics