Cogan, J D <br/><br/>
Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Nov 1994 
 - 1261-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0021-972X 
<br/><br/><label>Standard No.: </label>10.1210/jcem.79.5.7962317  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alleles<br/>Base Sequence<br/>Child<br/>DNA, Complementary--analysis<br/>Exons<br/>Female<br/>Genes, Dominant<br/>Genes, Recessive<br/>Growth Disorders--genetics<br/>Growth Hormone--analysis<br/>Humans<br/>Male<br/>Middle Aged<br/>Models, Genetic<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>RNA, Messenger--analysis<br/>Transcription, Genetic