Associated Papers
A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins.
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Frontiers in Pediatrics, 2024
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Supplement: Table1.xlsx › filter_variants
Whole-exome sequencing reveals POLR3B variants associated with progeria-related Wiedemann-Rautenstrauch syndrome.
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Italian Journal of Pediatrics, 2021
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Supplement: 13052_2021_1112_MOESM2_ESM.xlsx › Sheet1
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