APA

Warejko J. K., Schueler M., Vivante A., Tan W., Daga A., Lawson J. A., Braun D. A., Shril S., Amann K., Somers M. J. G., Rodig N. M., Baum M. A., Daouk G., Traum A. Z., Kim H. B., Vakili K., Porras D., Lock J., Rivkin M. J., Chaudry G., Smoot L. B., Singh M. N., Smith E. R., Mane S. M., Lifton R. P., Stein D. R., Ferguson M. A. & Hildebrandt F. (20190123). Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. : Hypertension (Dallas, Tex. : 1979).

Chicago

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 and Hildebrandt Friedhelm. 20190123. Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. : Hypertension (Dallas, Tex. : 1979).

Harvard

Warejko J. K., Schueler M., Vivante A., Tan W., Daga A., Lawson J. A., Braun D. A., Shril S., Amann K., Somers M. J. G., Rodig N. M., Baum M. A., Daouk G., Traum A. Z., Kim H. B., Vakili K., Porras D., Lock J., Rivkin M. J., Chaudry G., Smoot L. B., Singh M. N., Smith E. R., Mane S. M., Lifton R. P., Stein D. R., Ferguson M. A. and Hildebrandt F. (20190123). Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. : Hypertension (Dallas, Tex. : 1979).

MLA

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 and Hildebrandt Friedhelm. Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. : Hypertension (Dallas, Tex. : 1979). 20190123.