Two sisters resembling Gorlin–Chaudhry–Moss syndrome von Aravena, Teresa, Passalacqua, Cristóbal, Pizarro, Oscar, Aracena, Mariana

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Psychological and cognitive evaluation of autism in a patient with MOMO syndrome: a case report and literature review von Passalacqua, Cristóbal, García, Matías, Sepúlveda, Elisa, Toledo, Diego, Valencia, Matías, Arancibia, Marcelo

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A pigmentary skin defect is a new finding in Marshall-Smith syndrome von Passalacqua, Cristóbal, Melo, Camila, Martín, Luz María, Rojas, Francisca, Sanz, Patricia, Taucher, Silvia Castillo, Aranibar, Ligia

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Genetic markers in essential hypertension von Passalacqua, Cristóbal, Taucher, Silvia Castillo

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Molecular and genetic studies for hereditary colon cancer in two patients and their families von Aravena, Teresa, Passalacqua, Cristóbal, Castillo Taucher, Silvia

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Cáncer hereditario de colon: Aportes del diagnóstico genético molecular von ARAVENA, TERESA, PASSALACQUA, CRISTÓBAL, CASTILLO TAUCHER, SILVIA

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Psychological and cognitive evaluation of autism in a patient with MOMO syndrome: a case report and literature review von Cristóbal Passalacqua, Matías García, Elisa Sepúlveda, Diego Toledo, Matías Valencia, Marcelo Arancibia

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STAAR, a phase I/II study of isaralgagene civaparvovec (ST-920) gene therapy in adults with Fabry disease: Dose escalation phase results von Hopkin, Robert J., Ganesh, Jaya, Deegan, Patrick, Goker-Alpan, Ozlem, Bernat, John, Wilcox, William R., Pahl, Madeleine V., Whitley, Chester B., Hughes, Derralynn, Nicholls, Kathleen, Cao, Liching, Chen, Michael, Shiue, Lisa H., Bowden, Emma, Jaggumantri, Sravan, Passalacqua, Cristobal, Souberbielle, Bernard, Cockroft, Bettina M.

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Genetic markers in essential hypertension von Passalacqua, Cristóbal, Taucher, Silvia Castillo

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Marcadores genéticos en hipertensión esencial von PASSALACQUA, CRISTÓBAL, CASTILLO TAUCHER, SILVIA

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Cáncer hereditario de colon: Aportes del diagnóstico genético molecular von ARAVENA, TERESA, PASSALACQUA, CRISTÓBAL, CASTILLO TAUCHER, SILVIA

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METHODS FOR USE OF VIRAL VECTOR CONSTRUCTS FOR THE TREATMENT OF FABRY DISEASE von SOUBERBIELLE, Bernard, PASSALACQUA, Cristobal, HUSTON, Marshall

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METHODS FOR USE OF VIRAL VECTOR CONSTRUCTS FOR THE TREATMENT OF FABRY DISEASE von SOUBERBIELLE, Bernard, PASSALACQUA, Cristobal, HUSTON, Marshall

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METHODS FOR USE OF VIRAL VECTOR CONSTRUCTS FOR THE TREATMENT OF FABRY DISEASE von HUSTON, MARSHALL, SOUBERBIELLE, BERNARD, PASSALACQUA, CRISTOBAL

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METHODS FOR USE OF VIRAL VECTOR CONSTRUCTS FOR THE TREATMENT OF FABRY DISEASE von SOUBERBIELLE, Bernard, PASSALACQUA, Cristobal, HUSTON, Marshall

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A novel MEFV gene mutation (A511V) in a Chilean FMF patient von Akar, Nejat, Öztürk, Ayşenur, Arslan, Çiğdem, Akar, Ece, Taucher, Silvia Castillo, Passalacqua, Cristobal

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파브리병의 치료를 위한 바이러스 벡터 작제물의 사용 방법 von PASSALACQUA CRISTOBAL, HUSTON MARSHALL, SOUBERBIELLE BERNARD

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Consenso de la Rama de Genética de la Sociedad Chilena de Pediatría sobre las anomalías congénitas de mal pronóstico vital (ACMPV): Genetics Consensus Committee von Pardo Vargas, Rosa A, Aracena, Mariana, Aravena, Teresa, Cares, Carolina, Cortés, Fanny, Faundes, Víctor, Mellado, Cecilia, Passalacqua, Cristóbal, Sanz, Patricia, Castillo Taucher, Silvia

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Consenso de la Rama de Genética de la Sociedad Chilena de Pediatría sobre las anomalías congénitas de mal pronóstico vital (ACMPV) von Pardo Vargas, Rosa A., Aracena, Mariana, Aravena, Teresa, Cares, Carolina, Cortés, Fanny, Faundes, Víctor, Mellado, Cecilia, Passalacqua, Cristóbal, Sanz, Patricia, Castillo Taucher, Silvia

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Two sisters resembling Gorlin-Chaudhry-Moss syndrome von Aravena, Teresa, Passalacqua, Cristóbal, Pizarro, Oscar, Aracena, Mariana

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