Warejko, Jillian K <br/><br/>
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.  [electronic resource] 

 -  Hypertension (Dallas, Tex. : 1979)  04 2018 
 - 691-699 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>1524-4563 
<br/><br/><label>Standard No.: </label>10.1161/HYPERTENSIONAHA.117.10296  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Aorta, Abdominal--pathology<br/>Aortic Valve Stenosis--diagnosis<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Female<br/>Genetic Association Studies<br/>Humans<br/>Hypertension--diagnosis<br/>Jagged-1 Protein--genetics<br/>Male<br/>Mutation<br/>Neurofibromatoses--diagnosis<br/>Neurofibromin 1--genetics<br/>Pedigree<br/>Syndrome<br/>United States<br/>Exome Sequencing--methods