Targeted disruption of Pax1 defines its null phenotype and proves haploinsufficiency

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 15, 1998, Pages 8692-8697

  Wilm, Bettina ^a   Dahl, Edgar ^a,b   Peters, Heiko ^a   Balling, Rudi ^a   Imai, Kenji ^a  

^a INSTITUTE OF EPIDEMIOLOGY   (Germany)

^b Metagen Gesell F Genomforschung M   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; BONE DEVELOPMENT; CONFERENCE PAPER; EMBRYO DEVELOPMENT; GENE MUTATION; GENE TARGETING; HAPLOIDY; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SCAPULA; SKELETON MALFORMATION; SPINE; STERNUM;

ANIMALIA; MURINAE; RODENTIA; VERTEBRATA;

EID: 0032555158     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.15.8692     Document Type: Article

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