Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome

Cytogenetics and Cell Genetics

Volumn 90, Issue 3-4, 2000, Pages 285-290

  Doyle, J L ^a   DeSilva, U ^a   Miller, W ^b   Green, Eric D ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b The Pennsylvania State University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; DNA;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CHROMOSOME 7Q; CHROMOSOME DELETION; GENE DELETION; GENE LOCATION; GENE MAPPING; GENE SEQUENCE; GENETIC CODE; GENETIC ORGANIZATION; GENOME; HUMAN; HUMAN TISSUE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; WILLIAMS BEUREN SYNDROME;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CLONING, MOLECULAR; EXONS; EXPRESSED SEQUENCE TAGS; GENE EXPRESSION PROFILING; HUMANS; INTRONS; MICE; MOLECULAR SEQUENCE DATA; OPEN READING FRAMES; PHYSICAL CHROMOSOME MAPPING; PROTEINS; RNA SPLICE SITES; RNA, MESSENGER; SEQUENCE DELETION; SEQUENCE HOMOLOGY; WILLIAMS SYNDROME;

EID: 0034528516     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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