Melle, D <br/><br/>
Two distinct mutations at a single BamHI site in phenylketonuria.  [electronic resource] 

 -  Journal of medical genetics  Jan 1991 
 - 38-40 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.28.1.38  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Blotting, Southern<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 12<br/>Deoxyribonuclease BamHI<br/>Exons<br/>Female<br/>Genes, Recessive<br/>Genotype<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Phenylalanine Hydroxylase--genetics<br/>Phenylketonurias--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length