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

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https://hal-normandie-univ.archives-ouvertes.fr/hal-02360738
Contributor : Pascale Veber Connect in order to contact the contributor
Submitted on : Wednesday, November 13, 2019 - 8:55:23 AM
Last modification on : Tuesday, October 19, 2021 - 4:17:36 PM

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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, Wiley, 2019. ⟨hal-02360738⟩

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