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3. Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2). Khonsari RH; Ohazama A; Raouf R; Kawasaki M; Kawasaki K; Porntaveetus T; Ghafoor S; Hammond P; Suttie M; Odri GA; Sandford RN; Wood JN; Sharpe PT Hum Mol Genet; 2013 May; 22(9):1873-85. PubMed ID: 23390131 [TBL] [Abstract][Full Text] [Related]
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