María-Isabel Tejada
4PUBLICATIONS
4CO-AUTHORS
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Publications (4)
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|Feb 12, 2020
Molecular characterization of Spanish patients with MECP2 duplication syndrome.Ainhoa Pascual-Alonso, Laura Blasco, Silvia Vidal
|Jan 04, 2020
Non-syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies.María Isabel Tejada, Nekane Ibarluzea
|Nov 22, 2018
A novel nonsense homozygous variant in the NLGN1 gene found in a pair of monozygotic twin brothers with intellectual disability and autism.María-Isabel Tejada, Xabier Elcoroaristizabal, Nekane Ibarluzea
|Mar 04, 2016
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome.B Schönewolf-Greulich, M-I Tejada, K Stephens
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