Publications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (10)

2024

  1. Identification of copy-number variants in patients with overgrowth disorders

    Clinical Genetics, Vol. 106, Núm. 5, pp. 614-624

2022

  1. Extremely variable expressivity in Smith-Lemli-Opitz syndrome: Review of 4 cases

    Anales de Pediatria, Vol. 96, Núm. 3, pp. 253-255

2016

  1. Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

    Genetics in Medicine, Vol. 18, Núm. 12, pp. 1226-1234

2014

  1. Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta

    American Journal of Medical Genetics, Part A, Vol. 164, Núm. 5, pp. 1136-1142