Macera, M J <br/><br/>
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.  [electronic resource] 

 -  Prenatal diagnosis  Mar 2015 
 - 299-301 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>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.4456  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adult<br/>Chromosome Disorders--diagnosis<br/>Female<br/>Genome<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Oligonucleotide Array Sequence Analysis<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Sequence Analysis, DNA<br/>Translocation, Genetic