about
Complexity and diversity of F8 genetic variations in the 1000 genomesSuccessful Phenotype Improvement following Gene Therapy for Severe Hemophilia A in Privately Owned Dogs.A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.Phenotype-genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation.Identification of mutations in the F8 and F9 gene in families with haemophilia using targeted high-throughput sequencing.Mutational Profiles of and in a Cohort of Haemophilia A and Haemophilia B Patients in the Multi-ethnic Malaysian Population
P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Genetic testing in bleeding disorders
@ast
Genetic testing in bleeding disorders
@en
Genetic testing in bleeding disorders
@nl
type
label
Genetic testing in bleeding disorders
@ast
Genetic testing in bleeding disorders
@en
Genetic testing in bleeding disorders
@nl
prefLabel
Genetic testing in bleeding disorders
@ast
Genetic testing in bleeding disorders
@en
Genetic testing in bleeding disorders
@nl
P2093
P2860
P356
P1433
P1476
Genetic testing in bleeding disorders
@en
P2093
C de Brasi
J Oldenburg
O El-Maarri
P2860
P356
10.1111/HAE.12409
P478
20 Suppl 4
P577
2014-05-01T00:00:00Z