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Marcos Morey

Showing results (1-10 of 5) with videos related to

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Medicina Clinica|April 11, 2009
[Emergence of hyperparathyroidism in X-linked hypophosphatemic rickets: iatrogenic or genetic?]Bárbara Hernández García, Marcos Morey Villar, Ricardo Escorihuela Esteban, et al.
Molecular Genetics and Metabolism|April 17, 2015
Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]Marcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Molecular Genetics and Metabolism|June 8, 2013
A glimpse into past, present, and future DNA sequencingMarcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
BMC Medical Genetics|September 10, 2011
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation typeMarcos Morey, Lidia Castro-Feijóo, Jesús Barreiro, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Medicina Clinica|April 11, 2009
[Emergence of hyperparathyroidism in X-linked hypophosphatemic rickets: iatrogenic or genetic?]Bárbara Hernández García, Marcos Morey Villar, Ricardo Escorihuela Esteban, et al.
Molecular Genetics and Metabolism|April 17, 2015
Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24]Marcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Molecular Genetics and Metabolism|June 8, 2013
A glimpse into past, present, and future DNA sequencingMarcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Orphanet Journal of Rare Diseases|April 29, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disordersAna Fernández-Marmiesse, Marcos Morey, Merce Pineda, et al.
BMC Medical Genetics|September 10, 2011
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation typeMarcos Morey, Lidia Castro-Feijóo, Jesús Barreiro, et al.
Pageof 1