Polymorphic microsatellites and Wilson disease (WD)

American Journal of Human Genetics

Volumn 53, Issue 4, 1993, Pages 864-873

  Stewart, E A ^a   White, A ^a   Tomfohrde, J ^a   Osborne Lawrence, S ^a   Prestridge, L ^a   Bonne Tamir, B ^a   Scheinberg, I H ^a   St George Hyslop, P ^a   Giagheddu, M ^a   Kim , J W ^a   Seo, J K ^a   Lo, W H Y ^a   Ivanova Smolenskaya, I A ^a   Limborska, S A ^a   Cavalli Sforza, L L ^a   Farrer, L A ^a   Bowcock, A M ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 13Q; CHROMOSOME MAP; COPPER METABOLISM; DIAGNOSTIC ACCURACY; DNA POLYMORPHISM; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC MARKER; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; WILSON DISEASE;

ADOLESCENT; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 13; DNA PRIMERS; DNA, SATELLITE; FEMALE; GENETIC MARKERS; HEPATOLENTICULAR DEGENERATION; HUMAN; INFANT, NEWBORN; LINKAGE DISEQUILIBRIUM; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM (GENETICS); SEQUENCE TAGGED SITES; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027507834     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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