Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly
about
Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Whole exome sequencing identif ...... al contractural arachnodactyly
@ast
Whole exome sequencing identif ...... al contractural arachnodactyly
@en
type
label
Whole exome sequencing identif ...... al contractural arachnodactyly
@ast
Whole exome sequencing identif ...... al contractural arachnodactyly
@en
prefLabel
Whole exome sequencing identif ...... al contractural arachnodactyly
@ast
Whole exome sequencing identif ...... al contractural arachnodactyly
@en
P2093
P2860
P1433
P1476
Whole exome sequencing identif ...... al contractural arachnodactyly
@en
P2093
Baofeng Yu
Chunying Song
Hongxia Li
Huaixiu Wang
Jinjie Xue
Qinzhao Yuan
Weijing Meng
Xingping Guo
P2860
P2888
P356
10.1186/S12881-016-0355-6
P577
2016-12-03T00:00:00Z
P6179
1050327540