Associated Papers
Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants.
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A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels.
Yuan Y et al.
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36159980 (PubMed )
Supplement: Table1.XLSX › SNP
Genetic alterations and their therapeutic implications in epithelial ovarian cancer.
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Development and validation of a multigene variant profiling assay to guide targeted and immuno therapy selection in solid tumors.
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Plos One, 2021
33556149 (PubMed )
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