Kelberman, D <br/><br/>
Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).  [electronic resource] 

 -  Clinical endocrinology  Jan 2009 
 - 96-103 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2265 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2265.2008.03326.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Animals<br/>CHO Cells<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Cricetinae<br/>Cricetulus<br/>DNA Mutational Analysis<br/>Female<br/>Gene Deletion<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Hypopituitarism--genetics<br/>Infant<br/>Male<br/>Pedigree<br/>Pituitary Hormones--deficiency