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Updated: Jun 4, 2025

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产前诊断和分子细胞遗传分析纯染色体10p15.3微删除使用染色体微阵列分析

Na Zhang1, Nan Huang2, Yu'e Chen3

  • 1Prenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, Fujian Province, 362000, China.

BMC medical genomics
|December 19, 2024
PubMed
概括

这项研究报告了两个胎儿染色体10p15.3微删除综合征的病例,为基因型-表型相关性提供了新的见解. 它强调了与这种罕见疾病相关的轻微临床特征,包括语言障碍.

关键词:
10p15.3 微删除综合征 微删除综合征染色体微阵列分析发育迟缓的发展延迟型分析分析 型分析产前诊断 在产前诊断.

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