Associated Papers
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 IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactyly.
Yamoto K et al.
Human Mutation, 2017
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