Mallolas, J <br/><br/>
Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes.  [electronic resource] 

 -  Molecular genetics and metabolism  Jun 1999 
 - 156-61 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1006/mgme.1999.2862  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Genetic Carrier Screening<br/>Genotype<br/>Humans<br/>Male<br/>Mutation<br/>Phenotype<br/>Phenylalanine--blood<br/>Phenylalanine Hydroxylase--deficiency<br/>Phenylketonurias--blood<br/>Reference Values<br/>Tyrosine--blood