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A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux
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نویسنده
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Takai Rie ,Ohta Tohru
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منبع
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journal of human genetics - 2016 - دوره : 61 - شماره : 9 - صفحه:773 -774
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آدرس
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Health Sciences University of Hokkaido, Japan, Health Sciences University of Hokkaido, Japan
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Authors
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