Oligogenic Origin of Differences of Sex Development in Humans von Camats, Nuria, Fluck, Christa E., Audi, Laura

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Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin? von Camats, Núria, Fernández-Cancio, Mónica, Audí, Laura, Schaller, André, Flück, Christa E

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Molecular Aspects of Sex Development in Mammals: New Insight for Practice von Audi, Laura, Bertelloni, Silvano, Fluck, Christa E.

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The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD) von Granada, Maria Luisa, Audí, Laura

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The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD) von Granada, Maria Luisa, Audí, Laura

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Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease von Flück, Christa E., Audí, Laura, Fernández-Cancio, Mónica, Sauter, Kay-Sara, Martinez de LaPiscina, Idoia, Castaño, Luis, Esteva, Isabel, Camats, Núria

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Clinical usefulness of growth hormone secretion elicited by acute stimulation tests von Laura, Audí, Antonio, Carrascosa

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Decreased cell proliferation and higher oxidative stress in fibroblasts from Down Syndrome fetuses. Preliminary study von Gimeno, Amparo, García-Giménez, José Luis, Audí, Laura, Toran, Nuria, Andaluz, Pilar, Dasí, Francisco, Viña, José, Pallardó, Federico V.

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Clinical usefulness of growth hormone secretion elicited by acute stimulation tests von Audí, Laura, Carrascosa, Antonio

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Five-alpha-reductase type 2 deficiency in Spain von Fernández-Cancio, Mónica, Audí, Laura, Yeste, Diego

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Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype von Parween, Shaheena, Fernandez-Cancio, Monica, Benito-Sanz, Sara, Camats, Nuria, Rojas Velazquez, Maria Natalia, Lopez-Siguero, Juan-Pedro, Udhane, Sameer S., Kagawa, Norio, Flueck, Christa E., Audi, Laura, Pandey, Amit

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Intracellular Oxidant Activity, Antioxidant Enzyme Defense System, and Cell Senescence in Fibroblasts with Trisomy 21 von Rodriguez-Sureda, Victor, Vilches, Angel, Sanchez, Olga, Audi, Laura, Dominguez, Carmen

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Nutritional rickets: vitamin D, calcium, and the genetic make-up von El Kholy, Mohamed, Elsedfy, Heba, Fernández-Cancio, Monica, Hamza, Rasha Tarif, Amr, Nermine Hussein, Ahmed, Alaa Youssef, Toaima, Nadin Nabil, Audí, Laura

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A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene von Burget, Lukas, Parera, Laura Audí, Fernandez-Cancio, Monica, Gräni, Rolf, Henzen, Christoph, Flück, Christa E

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El laboratorio en el diagnóstico multidisciplinar del desarrollo sexual anómalo o diferente (DSD) von Granada, Maria Luisa, Audí, Laura

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A Novel Homozygous AMRH2 Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome von Fernández-Cancio, Mónica, Viswanath, Naveen, Puzhankara, Ramakrishnan, Valiyaprambil Pavithran, Praveen, Mora-Palma, Cristina, Camats, Núria, Audí, Laura, Benito-Sanz, Sara

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Growth Hormone (GH) Dose, But Not Exon 3-Deleted/Full-Length GH Receptor Polymorphism Genotypes, Influences Growth Response to Two-Year GH Therapy in Short Small-for-Gestational-Ag... von Carrascosa, Antonio, Audí, Laura, Esteban, Cristina, Fernández-Cancio, Mónica, Andaluz, Pilar, Gussinyé, Miquel, Clemente, María, Yeste, Diego, Albisu, María Angeles

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Development of Laboratory Investigations in Disorders of Sex Development von Audí, Laura, Camats, Núria, Fernández-Cancio, Mónica, Granada, María L.

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The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD): III) Biochemical and genetic markers in the 46,XYIV) Proposals for the diffe... von Granada, Maria Luisa, Audí, Laura

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Past Experiences of Adults with Disorders of Sex Development von GrApSIA, Audí, Laura

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