染色体微阵列技术检测父源性t（13；22）非平衡易位22q13缺失综合征一例及文献复习
林俊伟, 侯红瑛, 章钧
Single nucleotide polymorphisms array for detecting paternal t (13;22) unbalanced translocation 22q13 deletion syndrome: a case report and literature review
Lin Junwei, Hou Hongying, Zhang Jun
新医学
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2023, (11): 826
-831
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DOI: 10.3969/j.issn.0253-9802.2023.11.012
