Smith, S D <br/><br/>
Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene.  [electronic resource] 

 -  Journal of learning disabilities   
 - 512-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Twin Study 
<br/><br/><label>ISSN: </label>0022-2194 
<br/><br/><label>Standard No.: </label>10.1177/002221940103400604  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Chromosomes, Human, Pair 6<br/>Crossing Over, Genetic--genetics<br/>DNA Mutational Analysis<br/>Diseases in Twins--genetics<br/>Dyslexia--genetics<br/>Exons--genetics<br/>Female<br/>Genetic Heterogeneity<br/>Genetic Markers--genetics<br/>Humans<br/>Intelligence--genetics<br/>Linkage Disequilibrium--genetics<br/>Male<br/>Myelin Proteins<br/>Myelin-Associated Glycoprotein--genetics<br/>Myelin-Oligodendrocyte Glycoprotein<br/>Phenotype