Steffann, J
Hôpital Necker-Enfants Malades · Institut Necker Enfants Malades · Institut des Maladies Génétiques Imagine
3 papers on CoChatORCID 0000-0001-5259-4144
Most cited papers
- Verified
Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis
Steffann, J., Frydman, N., Gigarel, N., Burlet, P., Ray, P. F., Fanchin, R., Feyereisen, E., Kerbrat, V, Tachdjian, G., Bonnefont, J.-P., et al. (2006) · Journal of Medical Genetics
Prenatal Screening and DiagnosticsMitochondrial Function and Pathology
Cited by 145
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Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti
Bodemer, C., Diociaiuti, A., Hadj‐Rabia, S., Robert, M. P., Desguerre, I., Manière, M. ‐., de la Dure‐Molla, M., De Liso, P., Federici, M., Galeotti, A., et al. (2020) · Journal of the European Academy of Dermatology and Venereology
Genetic and rare skin diseases.Dermatology and Skin Diseases
Cited by 59
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Could Failure in Preimplantation Genetic Diagnosis Justify Editing the Human Embryo Genome?
Steffann, J., Jouannet, P., Bonnefont, J.-P., Chneiweiss, H., & Frydman, N. (2018) · Cell Stem Cell
Prenatal Screening and DiagnosticsCRISPR and Genetic Engineering
Cited by 47
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