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2. A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophy. Wang Y; Wen X; Shen XM; Di L; Sun Y; Li Y; Zhang S; Wen Q; Wang J; Duo J; Huang Y; Lu Y; Xu M; Wang M; Chen H; Zhu W; Da Y Neuromuscul Disord; 2024 Jun; 39():24-29. PubMed ID: 38714145 [TBL] [Abstract][Full Text] [Related]
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17. A DMD case caused by X chromosome rearrangement. Hu H; Yang XW; Cheng DH; Li XR; He WB; Hu X; Gao BD; Zhao XM; Zhang QJ; Du J; Liu JY; Lu GX; Ge L; Li W Yi Chuan; 2023 Jan; 45(1):88-95. PubMed ID: 36927641 [TBL] [Abstract][Full Text] [Related]
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20. An approach to rapid characterization of DMD copy number variants for prenatal risk assessment. Chin HL; O'Neill K; Louie K; Brown L; Schlade-Bartusiak K; Eydoux P; Rupps R; Farahani A; Boerkoel CF; Jones SJM Am J Med Genet A; 2021 Aug; 185(8):2541-2545. PubMed ID: 34018669 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]