Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder - Archive ouverte HAL Access content directly
Journal Articles American Journal of Medical Genetics Year : 2019

Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder

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hal-02360738 , version 1 (13-11-2019)

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  • HAL Id : hal-02360738 , version 1

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Pascale Saugier-Veber. Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder. American Journal of Medical Genetics, 2019. ⟨hal-02360738⟩
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