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J.AJHG.2019.04.013
J.AJHG.2019.04.013
http://dx.doi.org/10.1016/J.AJHG.2019.04.013
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
P356
Q92303053-52985710-BA08-4050-906E-C4BF3165CD5E
P356
J.AJHG.2019.04.013
http://dx.doi.org/10.1016/J.AJHG.2019.04.013