P. Navarrete-Meneses

Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations

A. González-del Angel, P. Pérez-Vera, C. Salas-Labadía, 2019, Orphanet Journal of Rare Diseases.

NF-κB and Its Regulators During Pregnancy

M. Cancino-Diaz, S. Rodríguez-Martínez, F. Gómez-Chávez, 2021, Frontiers in Immunology.

Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy

F. Marchetti, S. Frías, B. Molina, 2018, Environmental and molecular mutagenesis.

Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis

K. Buiting, P. Pérez-Vera, Samuel Gómez, 2014, Molecular Cytogenetics.

Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review

A. Martinez-Hernandez, P. Pérez-Vera, C. Salas-Labadía, 2022, BMC Medical Genomics.

UPD(14)mat and UPD(14)mat in concomitance with mosaic small supernumerary marker chromosome 14 in two new patients with Temple syndrome.

C. E. Villarroel, P. Pérez-Vera, C. Salas-Labadía, 2021, European Journal of Medical Genetics.

Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis

K. Buiting, P. Pérez-Vera, Samuel Gómez, 2014, Molecular Cytogenetics.

Interstitial deletion of 2q24.2: Further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction

J. Castrillo, S. Frías, Leda Torres, 2014, American journal of medical genetics. Part A.