Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
about
Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia.Violating the theory of single gene-single disorder: inhibitor development in hemophiliaSpectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene.
P2860
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@en
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@nl
type
label
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@en
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@nl
prefLabel
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@en
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@nl
P2093
P2860
P1433
P1476
Sequencing of the factor 8(F8) ...... Willebrand's disease type 2N.
@en
P2093
Caglayan H
El-Maarri O
Fidanci ID
P2860
P304
P356
10.1111/J.1365-2516.2006.01302.X
P577
2006-07-01T00:00:00Z