Nose, Osamu <br/><br/>
Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT).  [electronic resource] 

 -  Journal of pediatric endocrinology & metabolism : JPEM  04 2006 
 - 491-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0334-018X 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Body Height--drug effects<br/>Child<br/>Child, Preschool<br/>Dwarfism, Pituitary--genetics<br/>Female<br/>Homeodomain Proteins--genetics<br/>Hormone Replacement Therapy<br/>Human Growth Hormone--therapeutic use<br/>Humans<br/>Pedigree<br/>Pituitary Hormones--deficiency<br/>Point Mutation<br/>Recombinant Proteins--therapeutic use<br/>Thyroid Hormones--therapeutic use