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2018
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Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutations.
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S-EPMC5054609
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biostudies-literature
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Overexpression of the Cytokine BAFF and Autoimmunity Risk.
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S-EPMC5605835
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biostudies-literature
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Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
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S-EPMC6022848
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biostudies-literature
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