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A commentary on ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome
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نویسنده
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Kaname Tadashi ,Yanagi Kumiko
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منبع
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journal of human genetics - 2017 - دوره : 62 - شماره : 8 - صفحه:739 -740
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آدرس
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National Center for Child Health and Development, Department of Genome Medicine, Japan, National Center for Child Health and Development, Department of Genome Medicine, Japan
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Authors
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