TY  - GEN
AU  - Warejko,Jillian K
AU  - Schueler,Markus
AU  - Vivante,Asaf
AU  - Tan,Weizhen
AU  - Daga,Ankana
AU  - Lawson,Jennifer A
AU  - Braun,Daniela A
AU  - Shril,Shirlee
AU  - Amann,Kassaundra
AU  - Somers,Michael J G
AU  - Rodig,Nancy M
AU  - Baum,Michelle A
AU  - Daouk,Ghaleb
AU  - Traum,Avram Z
AU  - Kim,Heung Bae
AU  - Vakili,Khashayar
AU  - Porras,Diego
AU  - Lock,James
AU  - Rivkin,Michael J
AU  - Chaudry,Gulraiz
AU  - Smoot,Leslie B
AU  - Singh,Michael N
AU  - Smith,Edward R
AU  - Mane,Shrikant M
AU  - Lifton,Richard P
AU  - Stein,Deborah R
AU  - Ferguson,Michael A
AU  - Hildebrandt,Friedhelm
TI  - Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome
SN  - 1524-4563
PY  - 2019///0123
KW  - Adolescent
KW  - Aorta, Abdominal
KW  - pathology
KW  - Aortic Valve Stenosis
KW  - diagnosis
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Female
KW  - Genetic Association Studies
KW  - Humans
KW  - Hypertension
KW  - Jagged-1 Protein
KW  - genetics
KW  - Male
KW  - Mutation
KW  - Neurofibromatoses
KW  - Neurofibromin 1
KW  - Pedigree
KW  - Syndrome
KW  - United States
KW  - Exome Sequencing
KW  - methods
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1161/HYPERTENSIONAHA.117.10296
ER  -