CHARGE Syndrome: An Indonesian Case Report
Background: CHARGE syndrome is an autosomal dominant congenital and rare genetic disease.The prevalence of CHARGE syndrome approximately 1:12,000 births.In the previous study, the CHD7 gene mutation is responsible in about 2/3 cases of CHARGE syndrome. The syndrome associations consist of C-colobo...
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| Main Authors: | , , , |
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| Format: | EJournal Article |
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Faculty of Medicine, Universitas Diponegoro,
2017-06-23.
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