Hilger, Alina <br/><br/>
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.  [electronic resource] 

 -  European journal of human genetics : EJHG  Dec 2013 
 - 1377-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2013.58  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Anal Canal--abnormalities<br/>Animals<br/>Anus, Imperforate--genetics<br/>DNA Copy Number Variations--genetics<br/>Esophagus--abnormalities<br/>Female<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Karyotyping--methods<br/>Kidney--abnormalities<br/>Limb Deformities, Congenital--genetics<br/>Male<br/>Mice<br/>Radius--abnormalities<br/>Receptors, G-Protein-Coupled--genetics<br/>Spine--abnormalities<br/>Trachea--abnormalities