Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome.
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H. Soejima | H. Nishibori | A. Noguchi | Tsutomu Takahashi | S. Tsuchida | K. Higashimoto | H. Arai | Hiroyuki Adachi | I. Takahashi | Tomoo Ito | M. Masue | Hiroaki Tamura