A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family
about
A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
A novel IGF2/H19 domain tripli ...... ll syndrome in a single family
@en
type
label
A novel IGF2/H19 domain tripli ...... ll syndrome in a single family
@en
prefLabel
A novel IGF2/H19 domain tripli ...... ll syndrome in a single family
@en
P2093
P50
P356
P1476
A novel IGF2/H19 domain tripli ...... ll syndrome in a single family
@en
P2093
Agata Skórka
Marta Smyk
Monika Kugaudo
Robert Śmigiel
P356
10.1002/AJMG.A.37964
P577
2016-09-09T00:00:00Z