1. Biblioteca Digital - Universidad icesi

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Doble aneuploidía (trisomía X, trisomía 18) en una recién nacida con fenotipo de trisomía 18
Pachajoa Londoño, Harry Mauricio
1-Jul-2013
Prevalencia de defectos congénitos en Risaralda, 2010-2013
Montoya, Juan José; Quiceno, Sandra Lorena; Molano Hurtado, Jaime; León Castaneda, Olga Mercedes; Porras Hurtado, Gloria Liliana; Pachajoa Londoño, Harry Mauricio
1-Dec-2016
Artrogriposis múltiple congénita en gemelo monocoriónico biamniótico. Reporte de caso y revisión de la literatura
Ruíz Botero, Felipe; Saldarriaga Gil, Wilmar; Pachajoa Londoño, Harry Mauricio
1-Jan-2009
Mosaic trisomy 13 and a sacral appendage
Pachajoa Londoño, Harry Mauricio; Meza Escobar, Luis Enrique.
31-Jul-2013
Clinical and molecular characterisation of two siblings with fibrodysplasia ossificans progressiva, from the Colombian Pacific coast (South America)
Pachajoa Londoño, Harry Mauricio; Botero Ramírez, Andrés Felipe
8-Jun-2015
Novel PORCN mutation in a severe case of Focal Dermal Hypoplasia
Pachajoa Londoño, Harry Mauricio; Ruiz Botero, Felipe
1-May-2016
Syndromic microphthalmia-3 caused by a mutation on gene SOX2 in a Colombian male patient
Pachajoa Londoño, Harry Mauricio; Ramirez-Botero, Andrés Felipe
1-Nov-2016
Cyclopia with synophthalmia in a 27 weeks old fetus
Pachajoa Londoño, Harry Mauricio
1-Jan-2010
Siamese twins with craniofacial duplication and bilateral cleft lip/palate in a ceramic representation of the Chimú culture (Peru): a comparative analysis with a current case.
Pachajoa Londoño, Harry Mauricio; Rodríguez, Carlos Armando; Porras Hurtado, Gloria Liliana; Hernandez Amaris, María F.
1-Jun-2014

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