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Elsevier

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Analysis of Multiple Mutations in the hALG6 Gene in a Patient with Congenital Disorder of Glycosylation Ic

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Chromosomal aberrations in congenital bone marrow failure disorders—an early indicator for leukemogenesis?

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Response: Congenital Transcobalamin II Deficiency Due to Errors in RNA Editing

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Congenital Transcobalamin II Deficiency Due to Errors in RNA Editing

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