Simm, Diemud <br/><br/>
Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children.  [electronic resource] 

 -  Acta paediatrica (Oslo, Norway : 1992)  Jun 2009 
 - 1057-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1651-2227 
<br/><br/><label>Standard No.: </label>10.1111/j.1651-2227.2009.01236.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child Development<br/>Child, Preschool<br/>Codon, Nonsense<br/>Congenital Hypothyroidism--blood<br/>Female<br/>Fetal Blood<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Iodide Peroxidase--genetics<br/>Male<br/>Mutation, Missense<br/>Thyrotropin--blood<br/>Ultrasonography, Prenatal