The BCL7 gene family: Deletion of BCL7B in Williams syndrome

Gene

Volumn 224, Issue 1-2, 1998, Pages 35-44

  Jadayel, Dalal M ^a   Osborne, Lucy R ^b   Coignet, Lionel J a ^a   Zani, Valter J ^a   Tsui, Lap Chee ^b   Scherer, Stephen W ^b   Dyer, Martin J s ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

5' RACE; Gene expression; Hemizygous deletion; Translocation

Indexed keywords

AMINO TERMINAL SEQUENCE; ARTICLE; CELL DEATH; CELL DIFFERENTIATION; CELL PROLIFERATION; CHROMOSOME 7; CHROMOSOME TRANSLOCATION; GENE DELETION; GENE FUNCTION; GENE ISOLATION; GENE MAPPING; HOMOZYGOSITY; HUMAN; HUMAN CELL; MOLECULAR CLONING; MULTIGENE FAMILY; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; WILLIAMS BEUREN SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BRUGIA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 7; DNA PROBES; DROSOPHILA MELANOGASTER; GENE EXPRESSION; GENES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICROFILAMENT PROTEINS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; NEOPLASM PROTEINS; PROTEINS; RNA, MESSENGER; SEQUENCE ALIGNMENT; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID; TISSUE DISTRIBUTION; WILLIAMS SYNDROME;

BRUGIA MALAYI; CAENORHABDITIS ELEGANS; DROSOPHILA MELANOGASTER; MELANOGASTER;

EID: 0032509326     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00514-9     Document Type: Article

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