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- [38] C-terminal insertion deletion in Exon 12 of the nucleophosmin gene is present in ∼50% of AML's with normal cytogenetics JOURNAL OF MOLECULAR DIAGNOSTICS, 2007, 9 (05): : 671 - 671
- [39] Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49-51 deletion phenotype MOLECULAR GENETICS & GENOMIC MEDICINE, 2023, 11 (01):