Göllner, H <br/><br/>
Complex phenotype of mice homozygous for a null mutation in the Sp4 transcription factor gene.  [electronic resource] 

 -  Genes to cells : devoted to molecular & cellular mechanisms  Aug 2001 
 - 689-97 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1356-9597 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2443.2001.00455.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Cell Line<br/>Chromosome Mapping<br/>Cloning, Molecular<br/>DNA--metabolism<br/>Embryo, Mammalian--metabolism<br/>Embryonic and Fetal Development<br/>Female<br/>Gene Targeting<br/>Growth--physiology<br/>Growth Disorders--genetics<br/>Homozygote<br/>Male<br/>Mice<br/>Mice, Knockout<br/>Mutation<br/>Reproduction<br/>Sexual Maturation--physiology<br/>Sp4 Transcription Factor<br/>Tissue Distribution<br/>Transcription Factors--deficiency<br/>Zinc Fingers