Characterization of CDC45L: A gene in the 22q11.2 deletion region expressed during murine and human development

Mammalian Genome

Volumn 10, Issue 3, 1999, Pages 322-326

  Shaikh, Tamim H ^a   Gottlieb, Shoshanna ^a   Sellinger, Beatrice ^a   Chen, Feng ^b   Roe, Bruce A ^b   Oakey, Rebecca J ^a,c   Emanuel, Beverly S ^a,c   Budarf, Marcia L ^a,c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF OKLAHOMA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CLEFT PALATE; CONTROLLED STUDY; DIGEORGE SYNDROME; FETUS; GENE DELETION; GENE EXPRESSION; GENE MAPPING; HEART DISEASE; HUMAN; HUMAN CELL; HYPOCALCEMIA; HYPOSPADIAS; IMMUNE DEFICIENCY; KIDNEY AGENESIS; LEARNING DISORDER; LIMB MALFORMATION; MENTAL DEFICIENCY; MOUSE; NEURAL TUBE DEFECT; NONHUMAN; NUCLEOTIDE SEQUENCE; VELOCARDIOFACIAL SYNDROME;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CELL CYCLE PROTEINS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; DNA PRIMERS; DNA REPLICATION; DNA, COMPLEMENTARY; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; MICE; MOLECULAR SEQUENCE DATA; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0032801291     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900996     Document Type: Article

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