Associated Papers
Case report: Long term response to growth hormone in a child with Silver-Russell syndrome-like phenotype due to a novel paternally inherited IGF2 variant.
Ventresca S et al.
Frontiers in Endocrinology, 2024
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
Inoue T et al.
Clinical Epigenetics, 2020
IGF2 Mutations.
Masunaga Y et al.
The Journal of Clinical Endocrinology and Metabolism, 2020
Select a paper to view details