De Novo Mutation of Paternal IGF2 Gene Causing Silver–Russell Syndrome in a Sporadic Patient

Overview of attention for article published in Frontiers in Genetics, August 2017

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So far, Dimensions has found 27 publications that cite this research output.

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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

Article in Frontiers in Endocrinology (March 2024)

Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome

Article in Frontiers in Pediatrics (October 2022)

Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p

Article in Molecular Syndromology (May 2022)

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