ClinVar Genomic Variation As It Relates To Human Health - NCBI

Từ khóa » Chek2 C.1312g T

• NM_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr) AND Not Provided

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• CHEK2 Variants Associate With Hereditary Prostate Cancer - Nature

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• Using Co-segregation And Loss Of Heterozygosity Analysis To Define ...

• Functional Analysis Identifies Damaging CHEK2 Missense Variants ...

• [PDF] PALB2, CHEK2 And ATM Rare Variants And Cancer Risk

• Genetic And Epigenetic Analyses Guided By High Resolution Whole ...