Complementation Mapping of Skeletal and Central Nervous System Abnormalities in Mice of the piebald Deletion Complex

Genetics

Volumn 143, Issue 1, 1996, Pages 447-461

  O'brien, Timothy P ^a   Metallinos, Danika L ^a   Chen, Hsiupei ^a   Shin, Myung K ^a   Tilghman, Shirley M ^a  

^a PRINCETON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CENTRAL NERVOUS SYSTEM MALFORMATION; CHROMOSOME 14; CHROMOSOME DELETION; CONGENITAL HYDROCEPHALUS; CONTROLLED STUDY; DELETION MUTANT; EMBRYO; FEMALE; FETUS; GENE MAPPING; GENETIC COMPLEMENTATION; HOMEOBOX; MALE; MOUSE; NONHUMAN; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; SKELETON MALFORMATION; SPINAL CORD MALFORMATION; ZYGOSITY;

ABNORMALITIES, MULTIPLE; ALLELES; ANIMALS; ANIMALS, NEWBORN; BASE SEQUENCE; BRAIN; CHROMOSOME DELETION; CHROMOSOME MAPPING; CROSSES, GENETIC; DNA PRIMERS; FEMALE; FETUS; GENETIC COMPLEMENTATION TEST; GENETIC MARKERS; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HYDROCEPHALUS; MALE; MICE; MICE, INBRED C3H; MICE, INBRED STRAINS; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; SPINAL CORD; SPINE;

EID: 0029986393     PISSN: 00166731     EISSN: 19432631     Source Type: Journal    
DOI: 10.1093/genetics/143.1.447     Document Type: Article

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