Hess, Ora <br/><br/>
Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Nov 2007 
 - 4387-93 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-972X 
<br/><br/><label>Standard No.: </label>10.1210/jc.2007-0684  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Arabs<br/>Child<br/>Child, Preschool<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Genotype<br/>Human Growth Hormone--blood<br/>Humans<br/>Infant<br/>Insulin-Like Growth Factor I--metabolism<br/>Jews<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Pedigree<br/>Phenotype<br/>Twins