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authFullName_s : Ralf Werner
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Broadening of cohesinopathies: Exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype

Ilaria Parenti , Cristina Gervasini , Jelena Pozojevic , Luitgard Graul-Neumann , Jacopo Azzollini et al.
Clinical Epigenetics, 2016, 89 (1), pp.74-81. ⟨10.1111/cge.12564⟩
Journal articles hal-01117251v1
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Novel mosaic variants in two patients with Cornelia de Lange syndrome

Jelena Pozojevic , Ilaria Parenti , Luitgard Graul-Neumann , Sara Ruiz Gil , Erwan Watrin et al.
European Journal of Medical Genetics, 2018, 61 (11), pp.680-684. ⟨10.1016/j.ejmg.2017.11.004⟩
Journal articles hal-01812513v1

Expanding the clinical spectrum of the "HDAC8-phenotype" - Implications for molecular diagnostics, counselling and risk prediction

Ilaria Parenti , Cristina Gervasini , Jelena Pozojevic , Kerstin S. Wendt , Erwan Watrin et al.
Clinical Genetics, 2016, 89 (5), pp.564-573. ⟨10.1111/cge.12717⟩
Journal articles istex hal-01255865v1