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A case of severe developmental delay with pharyngeal anomaly due to a de novo translocation [46, XY, t(6;12)(q16;p12)].

K Yamada, T Ono,T Ohki,Y Yamada,N Ishihara,K Miura,T Kumagai,S Sonta,N Wakamatsu

AMERICAN JOURNAL OF HUMAN GENETICS（2002）

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