Konecki, D S <br/><br/>
Facilitation of hyperphenylalaninaemia phenotype assessment by genotype analysis.  [electronic resource] 

 -  European journal of pediatrics  Dec 1993 
 - 1048-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/BF01957239  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Metabolism, Inborn Errors--genetics<br/>Child<br/>Female<br/>Genotype<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Phenotype<br/>Phenylalanine--blood<br/>Phenylketonurias--genetics