Alatzoglou, Kyriaki S <br/><br/>
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Sep 2009 
 - 3191-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1945-7197 
<br/><br/><label>Standard No.: </label>10.1210/jc.2008-2783  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Genetic Testing<br/>Homeodomain Proteins--genetics<br/>Human Growth Hormone--deficiency<br/>Humans<br/>Infant<br/>Locus Control Region<br/>Mutation<br/>Pedigree<br/>Receptors, Neuropeptide--genetics<br/>Receptors, Pituitary Hormone-Regulating Hormone--genetics<br/>SOXB1 Transcription Factors--genetics