MOESM5 of Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer
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https://figshare.com/articles/dataset/MOESM5_of_Whole_exome_sequencing_and_single_nucleotide_polymorphism_array_analyses_to_identify_germline_alterations_in_genes_associated_with_testosterone_metabolism_in_a_patient_with_androgen_insensitivity_syndrome_and_early-onset_colorectal_cancer/4460429
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Additional file 5: Table S5. List of single nucleotide variants (SNVs) and small insertions and deletions (INDELs) detected in WES data of III.2 and III.3 subjects.
创建时间：
2016-12-16
