Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1

Genetics

Volumn 159, Issue 2, 2001, Pages 715-726

  Clark, Richard M ^a   Marker, Paul C ^a,e   Roessler, Erich ^b   Dutra, Amalia ^b   Schimenti, John C ^c   Muenke, Maximilian ^b   Kingsley, David M ^a,d  

^a STANFORD UNIVERSITY   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c JACKSON LABORATORY   (United States)

^d STANFORD UNIVERSITY   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN LMBR1; UNCLASSIFIED DRUG;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CHROMOSOME 7Q; CONTROLLED STUDY; FEMALE; GENE ACTIVITY; GENE CONTROL; GENE DELETION; GENE EXPRESSION; GENE LOSS; GENE MAPPING; GENE MUTATION; HUMAN; LIMB DEFECT; LIMB DEVELOPMENT; MALE; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL;

ALLELES; ANIMALS; BLOTTING, NORTHERN; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 7; HOMOZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LIMB DEFORMITIES, CONGENITAL; MEMBRANE PROTEINS; MICE; MUTATION; PHENOTYPE;

EID: 0034754554     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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