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pro vyhledávání: '"Afef Jalloul"'
Autor:
Rahma Touhami, Hajer Foddha, Eudeline Alix, Afef Jalloul, Soumaya Mougou-Zerelli, Ali Saad, Damien Sanlaville, Amel Haj Khelil
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Background: Psychomotor delay, epilepsy and dysmorphic features are clinical signs which are described in multiple syndromes due to chromosomal imbalances or mutations involving key genes implicated in the stages of Early Embryonic Development. In th
Externí odkaz:
https://doaj.org/article/1ff57692a4c2414a9253be9a59dfae02
