Institute of Pathology and Genetics (IPG) / Institut de Génétique et de Pathologie
Research facility
Location:
Charleroi,
Belgium (BE)
ISNI: 0000000405780894
ROR: https://ror.org/00zam0e96
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Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature (2020)
Carmignac V, Nambot S, Lehalle D, Callier P, Moortgat S, Benoit V, Ghoumid J, et al.
Journal article
Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum (2016)
Smogavec M, Cleall A, Hoyer J, Lederer D, Nassogne MC, Palmer EE, Deprez M, et al.
Journal article