Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome

Putoux, A.; Alqahtani, A.; Pinson, L.; Paulussen, A.D.; Michel, J.; Besson, A.; Mazoyer, S.; Borg, I.; Nampoothiri, S.; Vasiljevic, A.; Uwineza, A.; Boggio, D.; Champion, F.; Die-Smulders, C.E. de; Gardeitchik, T.; Putten, W.K. van; Perez, M.J.; Musizzano, Y.; Razavi, F.; Drunat, S.; Verloes, A.; Hennekam, R.; Guibaud, L.; Alix, E.; Sanlaville, D.; Lesca, G.; Edery, P.

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Publication year

2016

Source

Clinical Genetics, 90, 6, (2016), pp. 550-555

ISSN

0009-9163

DOI

https://doi.org/10.1111/cge.12781

Publication type

Article / Letter to editor

If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/168100

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