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Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing.
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Supplement: 41525_2024_453_MOESM2_ESM.xlsx › PredictedDominant_Rare0
Neonatal congenital leukemia caused by several missense mutations and AFF1-KMT2A fusion: A case report.
Qin B et al.
Oncology Letters, 2022
Pan-genomic characterization of high-risk pediatric papillary thyroid carcinoma.
Stenman A et al.
Endocrine-related Cancer, 2021
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