학술논문
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects
Document Type
Journal
Author
Bolkier, Yoav; Barel, Ortal; Marek-Yagel, Dina; Atias-Varon, Danit; Kagan, Maayan; Vardi, Amir; Mishali, David; Katz, Uriel; Salem, Yishay; Tirosh-Wagner, Tal; Jacobson, Jeffrey M.; Raas-Rothschild, Annick; Chorin, Odelia; Eliyahu, Aviva; Sarouf, Yarden; Shlomovitz, Omer; Veber, Alvit; Shalva, Nechama; Javasky, Elisheva; Ben Moshe, Yishay; Staretz-Chacham, Orna; Rechavi, Gideon; Mane, Shrikant; Anikster, Yair; Vivante, Asaf; Pode-Shakked, Ben
Source
Subject
Language
English
ISSN
14686244