A gene(s) for all-trans-retinoic acid-induced forelimb defects mapped and confirmed to marine chromosome 11

Genetics

Volumn 170, Issue 1, 2005, Pages 345-353

  Lee, Grace S ^a   Cantor, Rita M ^b   Abnoosian, Arin ^a   Park, Euisun ^a   Yamamoto, Mitsuko L ^a   Hovland Jr , David N ^c   Collins, Michael D ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c AMGEN INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOIC ACID;

ARTICLE; BONE DENSITY; BONE HOMEOSTASIS; BONE MASS; CHROMOSOME 11; CHROMOSOME 18; CHROMOSOME 4; ECTOPIC TISSUE; ECTRODACTYLY; EPISTASIS; FETUS; FINGER MALFORMATION; FORELIMB; GENE MAPPING; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HOMEOSTASIS; INBRED STRAIN; LIMB DEVELOPMENT; LIMB MALFORMATION; MECKEL SYNDROME; MOUSE; MOUSE STRAIN; MOUSE STRAIN C57BL 6N; MOUSE STRAIN SWV; NONHUMAN; PHENOTYPE; POLYDACTYLY; PRENATAL DRUG EXPOSURE; PRIORITY JOURNAL; STRAIN DIFFERENCE; SYNTENY;

ANIMALS; CHROMOSOME MAPPING; CROSSES, GENETIC; EPISTASIS, GENETIC; FEMALE; FORELIMB; HUMANS; INBREEDING; KERATOLYTIC AGENTS; LIMB DEFORMITIES, CONGENITAL; LOD SCORE; MALE; MICE; MICE, INBRED C57BL; PHENOTYPE; TRETINOIN;

EID: 20444369930     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: 10.1534/genetics.104.038620     Document Type: Article

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