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About this Medicine article
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome by Warejko, Jillian K.; Schueler, Markus; Vivante, Asaf; Tan, Weizhen; Daga, Ankana; Lawson, Jennifer A.; Braun, Daniela A.; Shril, Shirlee; Amann, Kassaundra; Somers, Michael J.G.; Rodig, Nancy M.; Baum, Michelle A.; Daouk, Ghaleb; Traum, Avram Z.; Kim, Heung Bae; Vakili, Khashayar; Porras, Diego; Lock, James; Rivkin, Michael J.; Chaudry, Gulraiz; Smoot, Leslie B.; Singh, Michael N.; Smith, Edward R.; Mane, Shrikant M.; Lifton, Richard P.; Stein, Deborah R.; Ferguson, Michael A.; Hildebrandt, Friedhelm is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Warejko, Jillian K.; Schueler, Markus; Vivante, Asaf; Tan, Weizhen; Daga, Ankana; Lawson, Jennifer A.; Braun, Daniela A.; Shril, Shirlee; Amann, Kassaundra; Somers, Michael J.G.; Rodig, Nancy M.; Baum, Michelle A.; Daouk, Ghaleb; Traum, Avram Z.; Kim, Heung Bae; Vakili, Khashayar; Porras, Diego; Lock, James; Rivkin, Michael J.; Chaudry, Gulraiz; Smoot, Leslie B.; Singh, Michael N.; Smith, Edward R.; Mane, Shrikant M.; Lifton, Richard P.; Stein, Deborah R.; Ferguson, Michael A.; Hildebrandt, Friedhelm
- Publisher
- Lippincott Williams and Wilkins; Ovid Technologies Wolters Kluwer -American Heart Association; Lippincott Williams & Wilkins Ltd.; Ovid Technologies (Wolters Kluwer Health) (ISSN 0194-911X)
- Published
- 2018
- Language
- EN
- Field
- Medicine (Health Sciences)