Jean-Baptiste Rivière
0000-0001-9144-4210
3 papers found
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Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome
Report on three additional patients and genotype–phenotype correlation in SLC25A22-related disorders group
Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing
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