Clark, R M <br/><br/>
Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1.  [electronic resource] 

 -  Genetics  Oct 2001 
 - 715-26 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0016-6731 
<br/><br/><label>Standard No.: </label>10.1093/genetics/159.2.715  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Blotting, Northern<br/>Chromosome Mapping<br/>Chromosomes, Artificial, Bacterial<br/>Chromosomes, Human, Pair 7<br/>Homozygote<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Limb Deformities, Congenital--genetics<br/>Membrane Proteins--genetics<br/>Mice<br/>Mutation<br/>Phenotype