Ting, Jason C <br/><br/>
Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.  [electronic resource] 

 -  Human mutation  Dec 2007 
 - 1225-35 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>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.20583  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Angelman Syndrome--genetics<br/>Beckwith-Wiedemann Syndrome--genetics<br/>Chromosome Deletion<br/>Female<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Nuclear Family<br/>Polymorphism, Single Nucleotide--genetics<br/>Prader-Willi Syndrome--genetics<br/>Pseudohypoparathyroidism--genetics<br/>Software<br/>Uniparental Disomy--genetics