One novel 2.43Kb deletion and one single nucleotide mutation of the INSR gene in a Chinese neonate with Rabson-Mendenhall syndrome.
about
One novel 2.43Kb deletion and one single nucleotide mutation of the INSR gene in a Chinese neonate with Rabson-Mendenhall syndrome.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh-hant
name
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@en
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@nl
type
label
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@en
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@nl
prefLabel
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@en
One novel 2.43Kb deletion and ...... th Rabson-Mendenhall syndrome.
@nl
P2093
P2860
P356
P1476
One Novel 2.43Kb Deletion and ...... ith Rabson-Mendenhall Syndrome
@en
P2093
Bingbing Wu
Hongbo Chen
Huijun Wang
Wenhao Zhou
Xiang Chen
Xinran Dong
P2860
P304
P356
10.4274/JCRPE.5080
P50
P577
2017-10-30T00:00:00Z