Boland, Elena <br/><br/>
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.  [electronic resource] 

 -  American journal of human genetics  Aug 2007 
 - 292-303 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/519999  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Agenesis of Corpus Callosum<br/>Animals<br/>Child<br/>Child, Preschool<br/>Chromosome Breakage<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 1<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Mice<br/>Microcephaly--genetics<br/>Proto-Oncogene Proteins c-akt--genetics<br/>Translocation, Genetic