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://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
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Additional file 4. Table S4: NIFG results for diagnosis of X-linked recessive disorders.
创建时间：
2022-07-27
