KUKOR Léna

Unilab > Consultation Génétique

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Main Referenced Co-authors

Bours, Vincent (4)

Bulk, Saskia (4)

Docampo Martínez, Elisa (3)

Bertoli, Sabrina (2)

Chatelain, Camille (2)

Main Referenced Keywords

Arachnodactyly (1); Arachnodactyly/diagnosis (1); Arachnodactyly/genetics (1); Arachnodactyly/pathology (1); Child (1);

Main Referenced Disciplines

Genetics & genetic processes (3)

Cardiovascular & respiratory systems (1)

Publications (total 4)

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KUKOR, L., BERTOLI, S., Bours, V., BULK, S., & DOCAMPO MARTINEZ, E. (16 February 2018). Ehlers-Danlos syndrome in the University Hospital of Liege [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. https://hdl.handle.net/2268/221744

Chatelain, C., KUKOR, L., Bailleux, S., Bours, V., Bulk, S., & Docampo Martínez, E. (February 2025). Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature. European Journal of Medical Genetics, 73, 104985. doi:10.1016/j.ejmg.2024.104985

https://hdl.handle.net/2268/341172

Peer Reviewed verified by ORBi

Chatelain, C., KUKOR, L., BULK, S., Bours, V., & Docampo Martínez, E. (12 April 2024). SKI missense variant c.539C>T p.(Thr180Met), a recurrent variant in Shprintzen-Goldberg syndrome: a case report and review of literature [Poster presentation]. Annual Symposium : Single cells, to care or not to care?, Leuven, Belgium.

https://hdl.handle.net/2268/316362

Kukor, L., BERTOLI, S., CREVECOEUR, J., Bours, V., & BULK, S. (21 April 2022). What does a Genetic Counsellor do in the University Hospital of Liège ? [Poster presentation]. BeSHG/NVHG Annual Genetics Symposium 2022.

https://hdl.handle.net/2268/299738

https://hdl.handle.net/2268/221744