ENDOMETRIOSIS FAMILIAR: REPORTE DE UNA FAMILIA CON HERENCIA MENDELIANA by Guillermo Lay-Son R, Arlette Adauy E, Hugo Salinas P, Silvia Castillo T

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Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies by Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

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Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies by Guillermo Lay‐Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

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Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies by Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

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Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients by Luis E. León, Felipe Benavides, Karena Espinoza, Cecilia Vial, Patricia Alvarez, Mirta Palomares, Guillermo Lay-Son, Macarena Miranda, Gabriela M. Repetto

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Exome Sequencing Identifies Genetic Variants Associated with Extreme Manifestations of the Cardiovascular Phenotype in Marfan Syndrome by Yanireth Jimenez, Cesar Paulsen, Eduardo Turner, Sebastian Iturra, Oscar Cuevas, Guillermo Lay-son, Gabriela M. Repetto, Marcelo Rojas, Juan F. Calderon

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Molecular analysis of the eighteen most frequent mutations in the BRCA1 gene in 63 Chilean breast cancer families by LILIAN JARA, SANDRA AMPUERO, EUDOCIA SANTIBÁÑEZ, LORENA SECCIA, JUAN RODRÍGUEZ, MARIO BUSTAMANTE, GUILLERMO LAY-SON, JOSÉ MANUEL OJEDA, JOSÉ MIGUEL REYES, RAFAEL BLANCO

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