Ramos, Helton E <br/><br/>
New cases of isolated congenital central hypothyroidism due to homozygous thyrotropin beta gene mutations: a pitfall to neonatal screening.  [electronic resource] 

 -  Thyroid : official journal of the American Thyroid Association  Jun 2010 
 - 639-45 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1557-9077 
<br/><br/><label>Standard No.: </label>10.1089/thy.2009.0462  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Congenital Hypothyroidism--genetics<br/>Consanguinity<br/>Diagnostic Errors<br/>Female<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Neonatal Screening<br/>Pedigree<br/>Thyrotropin--analysis<br/>Thyrotropin, beta Subunit--genetics