2018
- MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
https://link.springer.com/article/10.1007%2Fs10048-018- 0541
(publication Dr Smol et Ghoumid-CHU Lille) - SnijdersBlok2018_Article_DeNovoMutationsInMED13ACompone_1310_.pdf
2017
- ARTICLE - EUROPEAN JOURNAL OF MEDICAL GENETICS by Dr Reza ASADOLLAHI (Zurich)
Genotype-phenotype-evaluation-of-MED13L-defects-in-the_2017_European-Journal.pdf
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