Hasi, Minire <br/><br/>
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions.  [electronic resource] 

 -  Human genetics  Dec 2011 
 - 777-87 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>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-011-1020-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors--genetics<br/>Child<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 18<br/>Cohort Studies<br/>Facies<br/>Family<br/>Female<br/>Genotype<br/>Hemizygote<br/>Humans<br/>Hyperventilation--genetics<br/>Intellectual Disability--genetics<br/>Male<br/>Phenotype<br/>Syndrome<br/>Transcription Factor 4<br/>Transcription Factors--genetics