APA

Shalata A., Mahroom M., Milewicz D. M., Limin G., Kassum F., Badarna K., Tarabeih N., Assy N., Fell R., Cohen H., Nashashibi M., Livoff A., Azab M., Habib G., Geiger D., Weissbrod O. & Nseir W. (20190314). Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype. : Orphanet journal of rare diseases.

Chicago

Shalata Adel, Mahroom Mohammad, Milewicz Dianna M, Limin Gong, Kassum Fadi, Badarna Khader, Tarabeih Nader, Assy Nimmer, Fell Rona, Cohen Hector, Nashashibi Munir, Livoff Alejandro, Azab Muhammad, Habib George, Geiger Dan, Weissbrod Omer and Nseir William. 20190314. Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype. : Orphanet journal of rare diseases.

Harvard

Shalata A., Mahroom M., Milewicz D. M., Limin G., Kassum F., Badarna K., Tarabeih N., Assy N., Fell R., Cohen H., Nashashibi M., Livoff A., Azab M., Habib G., Geiger D., Weissbrod O. and Nseir W. (20190314). Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype. : Orphanet journal of rare diseases.

MLA

Shalata Adel, Mahroom Mohammad, Milewicz Dianna M, Limin Gong, Kassum Fadi, Badarna Khader, Tarabeih Nader, Assy Nimmer, Fell Rona, Cohen Hector, Nashashibi Munir, Livoff Alejandro, Azab Muhammad, Habib George, Geiger Dan, Weissbrod Omer and Nseir William. Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype. : Orphanet journal of rare diseases. 20190314.