E. Gerotina

Characterization of large deletions of the MECP2 gene in Rett syndrome patients by gene dosage analysis

J. Armstrong, M. Pineda, S. Vidal, 2019, Molecular genetics & genomic medicine.

CDKL5 in different atypical Rett syndrome variants: Description of the first eight patients from Spain

J. Armstrong, M. Pineda, J. Campistol, 2012, Journal of Pediatric Epilepsy.

[FOXG1, a new gene responsible for the congenital form of Rett syndrome].

M. Pineda, E. Gerotina, Ó. Sans-Capdevila, 2011, Revista de neurologia.

X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

N. Baena, G. Antiñolo, S. Gökben, 2019, Scientific Reports.

Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

N. Baena, G. Antiñolo, Gábor Csányi, 2017, Scientific Reports.

The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

N. Baena, G. Antiñolo, S. Gökben, 2017, Scientific Reports.

The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

N. Baena, G. Antiñolo, S. Gökben, 2017, Scientific Reports.