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
IGF2 Mutations.
Masunaga Y et al.
The Journal of Clinical Endocrinology and Metabolism, 2020
A new p.(Ile66Serfs*93) IGF2 variant is associated with pre- and postnatal growth retardation.
Rockstroh D et al.
European Journal of Endocrinology, 2019
Rare De Novo IGF2 Variant on the Paternal Allele in a Patient With Silver-Russell Syndrome.
Xia CL et al.
Frontiers in Genetics, 2019
De Novo Mutation of Paternal IGF2 Gene Causing Silver-Russell Syndrome in a Sporadic Patient.
Liu D et al.
Frontiers in Genetics, 2017
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