Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects

Added 86 days ago (03.09.2021)
Authors: Bolkier, Y., Barel, O., Marek-Yagel, D., Atias-Varon, D., Kagan, M., Vardi, A., Mishali, D., Katz, U., Salem, Y., Tirosh-Wagner, T., Jacobson, J. M., Raas-Rothschild, A., Chorin, O., Eliyahu, A., Sarouf, Y., Shlomovitz, O., Veber, A., Shalva, N., Javasky, E., Ben Moshe, Y., Staretz-Chacham, O., Rechavi, G., Mane, S., Anikster, Y., Vivante, A., Pode-Shakked, B.
Journal: JMG Online
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