Generation and comparative analysis of ∼3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome

Genome Research

Volumn 12, Issue 1, 2002, Pages 3-15

  DeSilva, Udaya ^a,d   Elnitski, Laura ^c   Idol, Jacquelyn R ^a   Doyle, Johannah L ^a   Gan, Weiniu ^b,e   Thomas, James W ^a   Schwartz, Scott ^c   Dietrich, Nicole L ^b   Beckstrom Sternberg, Stephen M ^a,b   McDowell, Jennifer C ^b   Blakesley, Robert W ^a,b   Bouffard, Gerard G ^a,b   Thomas, Pamela J ^b   Touchman, Jeffrey W ^a,b   Miller, Webb ^c   Green, Eric D ^a,b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c The Pennsylvania State University   (United States)

^d OKLAHOMA STATE UNIVERSITY   (United States)

^e CELERA GENOMICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACCURACY; CHROMOSOME 7Q; COMPARATIVE STUDY; COMPUTER PROGRAM; CONTROLLED STUDY; DNA FLANKING REGION; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CODE; GENETIC CONSERVATION; GENETIC MODEL; HUMAN; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PRIORITY JOURNAL; REVIEW; SEQUENCE DATABASE; WILLIAMS BEUREN SYNDROME;

ANIMALS; BASE COMPOSITION; CHROMOSOMES, HUMAN, PAIR 7; CONSERVED SEQUENCE; HUMANS; MICE; MOLECULAR SEQUENCE DATA; PHYSICAL CHROMOSOME MAPPING; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, NUCLEIC ACID; WILLIAMS SYNDROME;

RODENTIA;

EID: 0036141877     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.214802     Document Type: Review

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