Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients.
about
Current insights into the diagnosis and treatment of inherited bone marrow failure syndromes in China.A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing.
P2860
Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients.
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
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@ast
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@en
type
label
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@ast
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@en
prefLabel
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@ast
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@en
P2093
P2860
P356
P1433
P1476
Whole exome sequencing reveals ...... idual Fanconi anemia patients.
@en
P2093
Fengchun Yang
Huimin Zeng
Jianfeng Zhou
Lixian Chang
Miaomiao Li
Mingjiang Xu
Quanquan Zhou
Weiping Yuan
P2860
P2888
P356
10.1186/1755-8794-7-24
P577
2014-05-15T00:00:00Z
P5875
P6179
1032450834