Ishida, M <br/><br/>
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.  [electronic resource] 

 -  Clinical genetics  04 2018 
 - 870-879 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13189  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anencephaly--genetics<br/>Animals<br/>Disease Models, Animal<br/>Epistasis, Genetic<br/>Female<br/>Genetic Association Studies<br/>Humans<br/>Male<br/>Mice<br/>Mutation<br/>Neural Tube Defects--genetics<br/>Phenotype<br/>Pregnancy<br/>Skull--abnormalities<br/>Spinal Dysraphism--genetics<br/>Exome Sequencing