Bayram, Yavuz <br/><br/>
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  May 2015 
 - E808-14 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1945-7197 
<br/><br/><label>Standard No.: </label>10.1210/jc.2015-1150  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Basic Helix-Loop-Helix Transcription Factors--genetics<br/>Child<br/>Exome<br/>Female<br/>Homozygote<br/>Humans<br/>Hypogonadism--genetics<br/>Mutation