Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome

Mammalian Genome

Volumn 11, Issue 8, 2000, Pages 675-681

  Taylor Clelland, Catherine L ^a   Levy, Brynn ^b   McKie, Judith M ^c   Duncan, Alessandra M V ^d   Hirschhorn, Kurt ^b   Bancroft, Carter ^a  

^a MOUNT SINAI MEDICAL CENTER   (United States)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^c HAIRMYRES HOSPITAL   (United Kingdom)

^d MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONGENITAL HEART DISEASE; FACE MALFORMATION; GENE MAPPING; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; GENITAL MALFORMATION; GROWTH RETARDATION; HUMAN; MENTAL DEFICIENCY; MOLECULAR CLONING; NEURAL TUBE DEFECT; PHENOTYPE; SKELETON MALFORMATION; TRISOMY;

AMINO ACID SEQUENCE; BASE SEQUENCE; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; CLONING, MOLECULAR; DNA; DNA, COMPLEMENTARY; DNA-BINDING PROTEINS; EXONS; FEMALE; GENE EXPRESSION; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENES; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTRONS; MALE; MOLECULAR SEQUENCE DATA; RNA, MESSENGER; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME; TISSUE DISTRIBUTION; TRANSCRIPTION FACTORS; TRISOMY;

RODENTIA;

EID: 0033884820     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003350010142     Document Type: Article

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