Poudrier, J <br/><br/>
Genotyping of a case of tyrosinaemia type I with normal level of succinylacetone in amniotic fluid.  [electronic resource] 

 -  Prenatal diagnosis  Jan 1999 
 - 61-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1097-0223(199901)19:1<61::aid-pd455>3.0.co;2-#  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--diagnosis<br/>Amniotic Fluid--chemistry<br/>Female<br/>Genotype<br/>Heptanoates--analysis<br/>Heterozygote<br/>Humans<br/>Hydrolases--deficiency<br/>Mutation<br/>Pedigree<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Tyrosine--blood