Wilkie, A O <br/><br/>
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.  [electronic resource] 

 -  American journal of human genetics  Jun 1990 
 - 1127-40 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Animals<br/>Child<br/>Child, Preschool<br/>Chromosome Mapping<br/>Female<br/>Gene Expression Regulation<br/>Genes<br/>Genetic Linkage<br/>Globins--genetics<br/>Humans<br/>Hybrid Cells<br/>Infant<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation<br/>Syndrome<br/>Thalassemia--genetics