Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families

Human Genetics

Volumn 87, Issue 1, 1991, Pages 11-17

  Svensson, Elisabeth ^a   von Döbeln, Ulrika ^a   Hagenfeldt, Lars ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ADULT; ARTICLE; CHILD; DNA POLYMORPHISM; GENE LOCUS; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PHENOTYPE; PHENYLKETONURIA; PRIORITY JOURNAL; SWEDEN;

ALLELES; DNA; HAPLOTYPES; HETEROZYGOTE; HUMAN; INFANT, NEWBORN; MUTATION; PHENOTYPE; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PRENATAL DIAGNOSIS; SUPPORT, NON-U.S. GOV'T; SWEDEN;

EID: 0025801391     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF01213084     Document Type: Article

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