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Article

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.
Vermeer, A.M., van Engelen, K., Postma, A.V., Baars, M.J., Christiaans, I., De Haij, S., Klaassen, S. ORCID logoORCID: https://orcid.org/0000-0001-5925-9912, Mulder, B.J. and Keavney, B.
American Journal of Medical Genetics C 163 (3): 178-184. August 2013

Review

Emerging cellular and gene therapies for congenital anemias.
Ludwig, L.S. ORCID logoORCID: https://orcid.org/0000-0002-2916-2164, Khajuria, R.K. and Sankaran, V.G.
American Journal of Medical Genetics C 172C (4): 332-348. 12 December 2016

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