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3. VEGF, facteur tissulaire, marqueurs de la coagulation et de la fibrinolyse dans les malformations vasculaires à flux lent : étude prospective et impact du sirolimus

12. De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy

15. MyeLDM, le trait d’union des dyraphismes

16. Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephaly

19. Caractérisation clinique et génétique d’une nouvelle dysplasie ectodermique en mosaïque

25. Refining the phenotypical and mutational spectrum of Taybi‐Linder syndrome

28. Mutations activatrices de mTOR en mosaïque dans l’hypomélanose d’Ito avec mégalencéphalie

35. Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis

36. Fetal thrombotic vasculopathy is associated with thromboembolic events and adverse perinatal outcome but not with neurologic complications: A retrospective cohort study of 54 cases with a 3-year follow-up of children

41. Le propranolol dans les hémangiomes infantiles : résultats de l’étude adaptative de phase 2/3 internationale, randomisée, contrôlée multi-doses versus placebo

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