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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. and van Engelen, K. and Postma, A.V. and Baars, M.J. and Christiaans, I. and De Haij, S. and Klaassen, S. and 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. and Khajuria, R.K. and Sankaran, V.G.
American Journal of Medical Genetics C 172C (4): 332-348. 12 December 2016