Filges, I <br/><br/>
Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants.  [electronic resource] 

 -  Molecular human reproduction  Apr 2015 
 - 339-46 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2407 
<br/><br/><label>Standard No.: </label>10.1093/molehr/gau112  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormal Karyotype<br/>Abortion, Habitual--diagnosis<br/>Adult<br/>Exome<br/>Female<br/>Gene Expression<br/>Genetic Predisposition to Disease<br/>Genotype<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Meiosis<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Phospholipase C delta--genetics<br/>Pregnancy<br/>Receptors, Steroid--genetics<br/>Sequence Analysis, DNA<br/>Triploidy<br/>Oxysterol Binding Proteins