Additional file 4 of Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders
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https://springernature.figshare.com/articles/dataset/Additional_file_4_of_Noninvasive_fetal_genotyping_of_single_nucleotide_variants_and_linkage_analysis_for_prenatal_diagnosis_of_monogenic_disorders/20388419/1
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Additional file 4. Table S4: NIFG results for diagnosis of X-linked recessive disorders.
补充材料4 附表S4:用于X连锁隐性遗传病诊断的NIFG检测结果
提供机构:
Chen, Songchang; Yu, Feng; Zhou, Xuanyou; Wang, Xuefeng; Xu, Chenming; Zhang, Lanlan; Jiang, Zhengwen; Wu, Wenman; Zhang, Dazhi
创建时间:
2022-07-28



