3-M syndrome: a growth disorder associated with IGF2 silencing.
about
Identifying biological pathways that underlie primordial short stature using network analysis.Inhibition of HIV-1 assembly by coiled-coil domain containing protein 8 in human cells.A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene.Signaling pathways regulating cartilage growth plate formation and activity.Intergenic GWAS SNPs are key components of the spatial and regulatory network for human growth.Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children.
P2860
3-M syndrome: a growth disorder associated with IGF2 silencing.
description
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name
3-M syndrome: a growth disorder associated with IGF2 silencing.
@en
3-M syndrome: a growth disorder associated with IGF2 silencing.
@nl
type
label
3-M syndrome: a growth disorder associated with IGF2 silencing.
@en
3-M syndrome: a growth disorder associated with IGF2 silencing.
@nl
prefLabel
3-M syndrome: a growth disorder associated with IGF2 silencing.
@en
3-M syndrome: a growth disorder associated with IGF2 silencing.
@nl
P2093
P2860
P50
P356
P1476
3-M syndrome: a growth disorder associated with IGF2 silencing
@en
P2093
P2860
P304
P356
10.1530/EC-13-0065
P577
2013-11-11T00:00:00Z