CNRGHFrançois Lecoquierre et al.Confirmation and further delineation of the SMG9‐deficiency syndrome, a rare and severe developmental disorderAmerican Journal of Medical Genetics Part A 2019, vol. 179, issue 11doi: 10.1002/ajmg.a.61317 2019 Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary CiliaToutes les publicationsSpecialization of small non-conjugative plasmids in Escherichia coli according to their family types
