Mutagenesis strategies for identifying novel loci associated with disease phenotypes

Seminars in Cell and Developmental Biology

Volumn 14, Issue 1, 2003, Pages 19-24

  Brown, Steve D M ^a   Hardisty, Rachel E ^a  

^a MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

Author keywords

Ethylnitrosourea (ENU); Mouse mutagenesis; Otitis media with effusion (OME)

Indexed keywords

DNA; ETHYLNITROSOUREA;

ALAGILLE SYNDROME; ANIMAL MODEL; ANIRIDIA; ASPHYXIA; AXENFELD RIEGER ANOMALY; BEHAVIOR DISORDER; BIRTH DEFECT; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE MODEL; DNA MODIFICATION; DYSTROPHY; EYE DISEASE; EYE MALFORMATION; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENETIC DISORDER; GENOME; HEARING IMPAIRMENT; HERITABILITY; HUMAN; IRIS DISEASE; MALFORMATION SYNDROME; MAMMALIAN GENETICS; MATING; MOLECULAR CLONING; MOUSE; MOUSE MUTANT; MUTAGENESIS; MYDRIASIS; NEUROLOGIC DISEASE; NONHUMAN; ORGANOGENESIS; PERIPHERAL NEUROPATHY; PHENOTYPE; POINT MUTATION; REVIEW; RIEGER SYNDROME; SCREENING; SECRETORY OTITIS MEDIA;

MAMMALIA;

EID: 0037329757     PISSN: 10849521     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1084-9521(02)00168-4     Document Type: Review

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