Search Results - "Vidales Moreno, C."

Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata‐Scalisi, F., Vidales Moreno, C., Stock, F., Avendaño, A., Araque, D., Lacruz‐Rengel, M.A., Diociaiuti, A., Bellacchio, E., Callea, M.

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TSC2/PKD1 contiguous gene deletion syndrome by Llamas Velasco, S, Camacho Salas, A, Vidales Moreno, C, Ceballos Rodríguez, R M, Murcia García, F J, Simón de la Heras, R

“…The TSC2 gene responsible for Tuberous Sclerosis, is located in chromosome 16p 13.3, adjacent to the gene for autosomal dominant polycystic kidney disease. A…”
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Síndrome de deleción de genes contiguos TSC2/PKD1 by Llamas Velasco, S, Camacho Salas, A, Vidales Moreno, C, Ceballos Rodríguez, R.M, Murcia García, F.J, Simón de la Heras, R

“…Resumen El gen TSC2, responsable de la esclerosis tuberosa, se encuentra en el cromosoma 16p13.3, adyacente al gen de la poliquistosis renal autosómica…”
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Two novel mutations in the TSC 2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata‐Scalisi, F., Vidales Moreno, C., Stock, F., Avendaño, A., Araque, D., Lacruz‐Rengel, M.A., Diociaiuti, A., Bellacchio, E., Callea, M.

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Síndrome de genes contiguos TSC2/PKD1 by Cammarata-Scalisi, Francisco, Vidales Moreno, Concha, Zara-Chirinos, Carmen, Bracho, Ana, Pérez, Diomar

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Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata-Scalisi, F, Vidales Moreno, C, Stock, F, Avendaño, A, Araque, D, Lacruz-Rengel, M A, Diociaiuti, A, Bellacchio, E, Callea, M

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