Brock, Stefanie <br/><br/>
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1.  [electronic resource] 

 -  European journal of human genetics : EJHG  08 2018 
 - 1132-1142 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/s41431-018-0146-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Brain--diagnostic imaging<br/>Child<br/>Cognitive Dysfunction--genetics<br/>Female<br/>Heterozygote<br/>Humans<br/>Lissencephaly--genetics<br/>Male<br/>Microcephaly--genetics<br/>Mutation, Missense<br/>Phenotype<br/>Syndrome<br/>Tubulin--chemistry