Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans

Mammalian Genome

Volumn 7, Issue 9, 1996, Pages 639-643

  Rizzu, P ^a   Lindsay, E A ^a   Taylor, C ^b   O'Donnell, H ^b   Levy, A ^c   Scambler, P ^b   Baldini, A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c TIMONE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DGCR14 PROTEIN, HUMAN; NUCLEAR PROTEIN; PRIMER DNA; PROTEIN;

ADULT; AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CAENORHABDITIS ELEGANS; CHROMOSOME 22; CHROMOSOME MAP; COMPARATIVE STUDY; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; DIGEORGE SYNDROME; FACE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; HUMAN; KARYOTYPING; MOLECULAR GENETICS; MOUSE; MULTIPLE MALFORMATION SYNDROME; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY; SKULL; SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CAENORHABDITIS ELEGANS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; CONSERVED SEQUENCE; DIGEORGE SYNDROME; DNA PRIMERS; FACE; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICE; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; POLYMERASE CHAIN REACTION; PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; SKULL; SYNDROME;

EID: 0030240577     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900197     Document Type: Article

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