Phenylketonuria screening registry as a resource for population genetic studies.

Journal of medical genetics

Volumn 42, Issue 10, 2005, Pages

  Hannelius, U ^a   Lindgren, C M ^a   Melen E ^a   Malmberg, A ^a   von Dobeln, U ^a   Kere, J ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

PRIMER DNA;

ALLELE; BIOLOGICAL MODEL; CHEMISTRY; GENE DELETION; GENE FREQUENCY; GENETICS; HETEROZYGOTE; HUMAN; LABORATORY DIAGNOSIS; LETTER; METHODOLOGY; NEWBORN; NEWBORN SCREENING; PHENYLKETONURIA; POPULATION GENETICS; REGISTER; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; DNA PRIMERS; GENE DELETION; GENE FREQUENCY; GENETICS, POPULATION; HETEROZYGOTE; HUMANS; INFANT, NEWBORN; MODELS, GENETIC; NEONATAL SCREENING; PHENYLKETONURIAS; POLYMORPHISM, SINGLE NUCLEOTIDE; REGISTRIES; SPECIMEN HANDLING;

EID: 32544455442     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2005.032987     Document Type: Letter

References (0)