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Advances in Therapy|April 3, 2020
FGF23-Related Hypophosphataemic Bone DiseaseAntonio González-Meneses López
Advances in Therapy|April 3, 2020
Genetic Diagnosis of Rare Diseases: Past and PresentFeliciano Ramos-Fuentes, Antonio González-Meneses, Elisabet Ars, et al.
Medicine|March 12, 2019
Expanding the clinical and mutational spectrum of germline ABL1 mutations-associated syndrome: A case reportNereida Bravo-Gil, Irene Marcos, Antonio González-Meneses, et al.
Cytogenetic and Genome Research|May 25, 2016
Heterogeneity of a Constitutional Complex Chromosomal Rearrangement in 2qJavier Del Rey, Mónica Santos, Antonio González-Meneses, et al.
BMC Medical Genetics|September 24, 2010
Novel association of severe neonatal encephalopathy and Hirschsprung disease in a male with a duplication at the Xq28 regionRaquel M Fernández, Rocío Núñez-Torres, Antonio González-Meneses, et al.
Molecular Genetics and Metabolism Reports|June 17, 2021
Open-label phase 1/2 study of vestronidase alfa for mucopolysaccharidosis VIISimon Jones, Mahmut Coker, Antonio González-Meneses López, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Infantile systemic hyalinosis: a clinicopathological studyGermán Rodríguez Criado, Antonio González-Meneses, Manuela Cañadas, et al.
Case Reports in Genetics|November 8, 2014
Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13Javier Sánchez, Ana Peciña, Olga Alonso-Luengo, et al.
Orphanet Journal of Rare Diseases|September 6, 2024
VUS next in rare diseases? Deciphering genetic determinants of biomolecular condensationMaría Heredia-Torrejón, Raúl Montañez, Antonio González-Meneses, et al.
Medicine|July 20, 2018
Diagnosis and follow-up of patients with Hunter syndrome in Spain: A Delphi consensusLuis González-Gutiérrez-Solana, Encarnación Guillén-Navarro, Mireia Del Toro, et al.
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