Olivier Alibeu
Imagine Institute for Genetic Diseases
14 papers found
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Loss of ARHGEF1 causes a human primary antibody deficiency
Download from doi.orgMED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence
Download from api.wiley.comMutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
Download from www.nature.comMutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability
Download from www.ncbi.nlm.nih.govCE-SSCP and CE-FLA, simple and high-throughput alternatives for fungal diversity studies
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