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JMEDGENET-2014-102964
JMEDGENET-2014-102964
http://dx.doi.org/10.1136/JMEDGENET-2014-102964
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P356
Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
P356
JMEDGENET-2014-102964
http://dx.doi.org/10.1136/JMEDGENET-2014-102964