Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders.
Kaori Hara-IsonoAkie NakamuraTomoko FukeTakanobu InoueSayaka KawashimaKeiko MatsubaraShinichiro SanoKazuki YamazawaMaki FukamiTsutomu OgataMasayo KagamiPublished in: The Journal of clinical endocrinology and metabolism (2022)
We clarified the contribution of PCNVs and pathogenic variants to SGA-SS without IDs. Comprehensive molecular analyses, including copy number analysis and multigene sequencing, should be considered for patients with unknown SGA-SS etiology.