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5 results for Morey,+Marcos

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ArticlesPeer ReviewedFull Text
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 type
Author / Creator:Morey, Marcos ; Castro-Feijóo, Lidia ; Barreiro, Jesús ; Cabanas, Paloma ; Pombo, Manuel ; Gil, Marta ; Bernabeu, Ignacio ; Díaz-Grande, José M ; Rey-Cordo, Lourdes ; Ariceta, Gema ; Rica, Itxaso ; Nieto, José ; Vilalta, Ramón ; Martorell, Loreto ; Vila-Cots, Jaime ; Aleixandre, Fernando ; Fontalba, Ana ; Soriano-Guillén, Leandro ; García-Sagredo, José M ; García-Miñaur, Sixto ; Rodríguez, Berta ; Juaristi, Saioa ; García-Pardos, Carmen ; Martínez-Peinado, Antonio ; Millán, José M ; Medeira, Ana ; Moldovan, Oana ; Fernandez, Angeles ; Loidi, Lourdes
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2011-09, Vol.12 (1), p.116-116, Article 116
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Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders
Author / Creator:Fernández-Marmiesse, Ana ; Morey, Marcos ; Pineda, Merce ; Eiris, Jesús ; Couce, Maria ; Castro-Gago, Manuel ; Fraga, Jose ; Lacerda, Lucia ; Gouveia, Sofia ; Pérez-Poyato, Maria ; Armstrong, Judith ; Castiñeiras, Daisy ; Cocho, Jose A
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2014-04, Vol.9 (1), p.59-59
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ArticlesPeer ReviewedFull Text
Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25
Author / Creator:Morey, Marcos ; Castro-Feijóo, Lidia ; Barreiro, Jesús ; Cabanas, Paloma ; Pombo, Manuel ; Gil, Marta ; Bernabeu, Ignacio ; Díaz-Grande, José M ; Rey-Cordo, Lourdes ; Ariceta, Gema ; Rica, Itxaso ; Nieto, José ; Vilalta, Ramón ; Martorell, Loreto ; Vila-Cots, Jaime ; Aleixandre, Fernando ; Fontalba, Ana ; Soriano-Guillén, Leandro ; García-Sagredo, José M ; García-Miñaur, Sixto ; Rodríguez, Berta ; Juaristi, Saioa ; García-Pardos, Carmen ; Martínez-Peinado, Antonio ; Millán, José M ; Medeira, Ana ; Moldovan, Oana ; Fernandez, Angeles ; Loidi, Lourdes
Publisher:BioMed Central Ltd
Journal title:BMC medical genetics, 2011-09, Vol.12, p.116
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Access ebook if you are in the Library. Registered NSW residents may log in from home.
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Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25.sub.2 D serum levels are associated with PHEX mutation type
Author / Creator:Morey, Marcos ; Castro-Feijóo, Lidia ; Barreiro, Jesús ; Cabanas, Paloma ; Pombo, Manuel ; Gil, Marta ; Bernabeu, Ignacio ; Díaz-Grande, José M ; Rey-Cordo, Lourdes ; Ariceta, Gema ; Rica, Itxaso ; Nieto, José ; Vilalta, Ramón ; Martorell, Loreto ; Vila-Cots, Jaime ; Aleixandre, Fernando ; Fontalba, Ana ; Soriano-Guillén, Leandro ; García-Sagredo, José M ; García-Miñaur, Sixto ; Rodríguez, Berta ; Juaristi, Saioa ; García-Pardos, Carmen ; Martínez-Peinado, Antonio ; Millán, José M ; Medeira, Ana ; Moldovan, Oana ; Fernandez, Angeles ; Loidi, Lourdes
Publisher:BioMed Central Ltd
Journal title:BMC medical genetics, 2011-09, Vol.12, p.116
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ArticlesPeer ReviewedFull Text
Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2 D serum levels are associated with PHEX mutation type
Author / Creator:Morey, Marcos ; Castro-Feijóo, Lidia ; Barreiro, Jesús ; Cabanas, Paloma ; Pombo, Manuel ; Gil, Marta ; Bernabeu, Ignacio ; Díaz-Grande, José M ; Rey-Cordo, Lourdes ; Ariceta, Gema ; Rica, Itxaso ; Nieto, José ; Vilalta, Ramón ; Martorell, Loreto ; Vila-Cots, Jaime ; Aleixandre, Fernando ; Fontalba, Ana ; Soriano-Guillén, Leandro ; García-Sagredo, José M ; García-Miñaur, Sixto ; Rodríguez, Berta ; Juaristi, Saioa ; García-Pardos, Carmen ; Martínez-Peinado, Antonio ; Millán, José M ; Medeira, Ana ; Moldovan, Oana ; Fernandez, Angeles ; Loidi, Lourdes
Publisher:London: BioMed Central
Journal title:BMC medical genetics, 2011-01, Vol.12, p.116
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.

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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 type

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Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders

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Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25

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Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25.sub.2 D serum levels are associated with PHEX mutation type

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Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2 D serum levels are associated with PHEX mutation type

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