Résultat de recherche

FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model.

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Signaling Pathways in Bone Development and Their Related Skeletal Dysplasia.

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Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy.

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Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals.

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Repurposing of the multiciliation gene regulatory network in fate specification of Cajal-Retzius neurons

Matthieu Moreau, Yoann Saillour, Vicente Elorriaga, Amaia OCHANDORENA SAA , Alessandra Pierani, Frédéric Causeret

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