开拓新领域:探索1p36微删除中的de novo染色体重组

Mariam M Al Eissa1,2, Raniah S Alotibi3,4, Amerh S Alqahtani5

  • 1Department of Medicne, Medical School, AlFaisal University, Riyadh, Saudi Arabia.

概括

本病例报告在神经发育迟缓的患者中发现了两种致病性染色体结构变异 (SV):1p36微删除和2p35.3微重复. 这些发现突出了SVs在遗传疾病中的复杂相互作用.

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