[XLS] CHBMP US Database - CDC
A .gov website belongs to an official government organization in the United States.
Secure .gov websites use HTTPSA lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.
The page you're looking for was not found.
Please try the CDC archives or the A-Z index.
Search CDC.gov
SearchThe page you were looking for has moved.
You will be automatically redirected to the new location in 10 seconds or you can click here to go to link.
Please update any bookmarks you may have saved for this page.
The page you were looking for has moved.
Please see:
Please update any bookmarks you may have saved for this page.
The page you were looking for has moved to archive.cdc.gov.
You will be automatically redirected to the new location in 10 seconds or you can click here to go to link.
Please update any bookmarks you may have saved for this page.
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 ...
-
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 ...
-
Genotype-Phenotype Heterogeneity In Haemophilia - IntechOpen
-
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