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RMND1 and PLN variants are the underlying cause of Perrault‐like syndrome and cardiac anomalies in a patient by Xiaoli Du, Cara L. Barnett, Kimberly M. Widmeyer, Xinjian Wang, Diana S. Brightman, Carolee W. Noonan, Kathryn N. Weaver, Robert J. Hopkin, Yaning Wu
Published 2024-11-01
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Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease by Laura B. Oehlman, Laura B. Oehlman, Laura B. Oehlman, Alexander R. Opotowsky, Alexander R. Opotowsky, Kathryn N. Weaver, Kathryn N. Weaver, Kathryn N. Weaver, Nicole M. Brown, Nicole M. Brown, Cara L. Barnett, Erin M. Miller, Erin M. Miller, Erin M. Miller, Hua He, Amy R. Shikany
Published 2024-05-01
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