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Genetic variants in NHEJ1 and related DNA repair disorders: insights into phenotypic heterogeneity and links to hypoplastic myelodysplastic syndromes and familial hematological malignancies susceptibility
3월 19, 2025
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Yeonho Kang
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Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program
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Situs Inversus in an Infant With Hypomandibular Faciocranial Syndrome: Clinical Overlap With the Agnathia-Otocephaly Complex
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