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Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.
Palma Milla C, Lezana Rosales JM, López Montiel J, Andrés Garrido LD, Sánchez Linares C, Carmona Tamajón S, Torres Fernández C, Sánchez González P, Franco Freire S, Benito López C, López Siles J. Palma Milla C, et al. Among authors: lopez siles j. Ann Hum Genet. 2018 Nov;82(6):425-436. doi: 10.1111/ahg.12272. Epub 2018 Jul 16. Ann Hum Genet. 2018. PMID: 30014477
Hyperinsulinemic hypoglycemia in a patient with an intragenic NSD1 mutation.
Carrasco Salas P, Palma Milla C, Lezana Rosales JM, Benito C, Franco Freire S, López Siles J. Carrasco Salas P, et al. Among authors: lopez siles j. Am J Med Genet A. 2016 Feb;170A(2):544-546. doi: 10.1002/ajmg.a.37440. Epub 2015 Oct 21. Am J Med Genet A. 2016. PMID: 26487424 No abstract available.
The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes.
Garcia Rodriguez R, Garcia Cruz L, Novoa Medina Y, Garcia Delgado R, Perez Gonzalez J, Palma Milla C, Lopez Siles J, Medina Castellano M, Garcia Hernandez JA, Santana Rodriguez A. Garcia Rodriguez R, et al. Among authors: lopez siles j. Prenat Diagn. 2019 May;39(6):415-419. doi: 10.1002/pd.5451. Epub 2019 Apr 26. Prenat Diagn. 2019. PMID: 30900264 Review.
[Influenza virus in pediatrics. A reason for hospitalization].
Cruz-Cañete M, Moreno-Pérez D, Jurado-Ortiz A, García-Martín FJ, López-Siles J, Olalla-Martín L. Cruz-Cañete M, et al. Among authors: lopez siles j. Enferm Infecc Microbiol Clin. 2007 Mar;25(3):177-83. doi: 10.1157/13099369. Enferm Infecc Microbiol Clin. 2007. PMID: 17335696 Spanish.