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Author/Creator Warejko, Jillian K.

2. Mutations in WDR4 as a new cause of Galloway–Mowat syndrome. Issue 11 (6th August 2018)

Authors:
Braun, Daniela A.; Shril, Shirlee; Sinha, Aditi; Schneider, Ronen; Tan, Weizhen; Ashraf, Shazia; Hermle, Tobias; Jobst‐Schwan, Tilman; Widmeier, Eugen; Majmundar, Amar J.; Daga, Ankana; Warejko, Jillian K.; Nakayama, Makiko; Schapiro, David; Chen, Jing; Airik, Merlin; Rao, Jia; Schmidt, Johanna M...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 11(2018)
Page Start:
2460
Record Type:
Journal Article
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4. Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. Issue 4 (April 2018)

Authors:
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; ...
Journal:
Hypertension
Issue:
Volume 71:Issue 4(2018:Apr.)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗