Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.
Mansfield, E S
Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status. [electronic resource] - Molecular and cellular probes Aug 1993 - 311-24 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0890-8508
10.1006/mcpr.1993.1045 doi
Adolescent
Adult
Base Sequence
DNA Primers
Female
Genetic Linkage
Heterozygote
Humans
Hypoxanthine Phosphoribosyltransferase--genetics
Introns--genetics
Lesch-Nyhan Syndrome--diagnosis
Male
Molecular Sequence Data
Multigene Family
Pedigree
Point Mutation--genetics
Polymerase Chain Reaction--methods
Polymorphism, Genetic
Repetitive Sequences, Nucleic Acid--genetics
Sequence Analysis, DNA
Sequence Deletion
Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status. [electronic resource] - Molecular and cellular probes Aug 1993 - 311-24 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0890-8508
10.1006/mcpr.1993.1045 doi
Adolescent
Adult
Base Sequence
DNA Primers
Female
Genetic Linkage
Heterozygote
Humans
Hypoxanthine Phosphoribosyltransferase--genetics
Introns--genetics
Lesch-Nyhan Syndrome--diagnosis
Male
Molecular Sequence Data
Multigene Family
Pedigree
Point Mutation--genetics
Polymerase Chain Reaction--methods
Polymorphism, Genetic
Repetitive Sequences, Nucleic Acid--genetics
Sequence Analysis, DNA
Sequence Deletion