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