NM_000133.3(F9):c.316G>A (p.Gly106Ser) AND Multiple Conditions
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See more...Từ khóa » F9 C.316g A
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NM_000133.3(F9):c.316G>A (p.Gly106Ser) AND Hereditary Factor ...
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List Of Variants In Gene F9 Studied For Hemophilia B - ClinVar Miner
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In Depth Mutation Analysis: C.316G>C (p.Gly106Arg) - Factor IX ...
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[XLS] CHBMP US Database - CDC
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Mutation Analysis Of A Cohort Of US Patients With ... - CDC Stacks
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Mutation Analysis Of A Cohort Of US Patients ... - Wiley Online Library
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Mutation Analysis Of A Cohort Of US Patients With Hemophilia B - Li
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Noninvasive Detection Of F8 Int22h-related Inversions And Sequence ...
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Genotype-Phenotype Heterogeneity In Haemophilia - IntechOpen
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Low Frequency Of Treatable Pediatric Disease Alleles In GnomAD
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Splicing Dysregulation Contributes To The Pathogenicity Of Several F9 ...
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[PDF] Splicing Dysregulation Contributes To The Pathogenicity Of Several ...
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Factor IX Gene (F9) Variant Database