Search Results - Gonzalez, V.
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Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum by Puig-Hervás, M., Temtamy, S., Aglan, M., Valencia, M., Martínez-Glez, V., Ballesta-Martínez, M., López-González, V., Ashour, A., Amr, K., Pulido, V., Guillén-Navarro, E., Lapunzina, P., Caparrós-Martín, Jose, Ruiz-Perez, V.
Published 2012Get full text
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Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta by Caparrós-Martín, Jose, Aglan, M., Temtamy, S., Otaify, G., Valencia, M., Nevado, J., Vallespin, E., Del Pozo, A., Prior de Castro, C., Calatrava-Ferreras, L., Gutierrez, P., Bueno, A., Sagastizabal, B., Guillen-Navarro, E., Ballesta-Martinez, M., Gonzalez, V., Basaran, S., Buyukoglan, R., Sarikepe, B., Espinoza-Valdez, C., Cammarata-Scalisi, F., Martinez-Glez, V., Heath, K., Lapunzina, P., Ruiz-Perez, V.
Published 2017Get full text