Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications.
Idske C L Kremer HovingaJacques C GiltaySaskia N van der CrabbenAnja SteylsHetty J van der KampAimée D C PaulussenPublished in: Clinical endocrinology (2018)
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