Rochiccioli, P <br/><br/>
[Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes].  [electronic resource] 

 -  Archives francaises de pediatrie  Jan 1974 
 - 25-36 p.  digital 
<br/><br/> Publication Type: Clinical Trial; English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>0003-9764 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations<br/>Chromosome Disorders<br/>Clinical Trials as Topic<br/>Consanguinity<br/>Diiodotyrosine--urine<br/>Female<br/>Genes, Recessive<br/>Goiter--etiology<br/>Heterozygote<br/>Humans<br/>Hypothyroidism--diagnosis<br/>Iodine--metabolism<br/>Iodine Radioisotopes<br/>Male<br/>Metabolism, Inborn Errors--complications<br/>Methods<br/>Thyroid Function Tests<br/>Thyroid Hormones--biosynthesis