Additional file 5 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_5_of_Noninvasive_fetal_genotyping_of_single_nucleotide_variants_and_linkage_analysis_for_prenatal_diagnosis_of_monogenic_disorders/20388422/1
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Additional file 5. Table S5: NIFG results for diagnosis of autosomal recessive disorders.
补充文件5：表S5：用于常染色体隐性遗传病诊断的NIFG检测结果
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figshare
创建时间：
2022-07-28
