A Patient with Bone Fragility, Multiple Fractures, Osteosarcoma, and the Variant c.143A>G in the IFITM5 Gene: A Case Report by Pachajoa H, Giraldo-Ocampo S

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2q37 deletion syndrome in a Colombian patient with macrocephaly: a case report by Sebastian Giraldo-Ocampo, Harry Pachajoa

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A Novel POGZ Variant in a Patient with Intellectual Disability and Obesity by Giraldo-Ocampo S, Pacheco-Orozco RA, Pachajoa H

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Caracterización molecular de las variantes del virus de Epstein-Barr detectadas en la cavidad oral de adolescentes de Cali, Colombia by Daniela Arturo-Terranova, Sebastián Giraldo-Ocampo, Andrés Castillo

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Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1 by Perafan-Valdes L, Giraldo-Ocampo S, Lores J, Pachajoa H

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Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies by Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J

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Glomerulonefritis rápidamente progresiva secundaria a vasculitis pauciinmune, entidad poco frecuente: caso clínico y revisión de la literatura by Christian Camilo Giraldo Ocampo, Maria Fernanda Jimenez Bejarano, Jhon Serna Flórez

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Modelo de proximidad espacial para definir sitios de muestreo en redes urbanas de calidad de aire by Libardo A. Londoño-Ciro, Julio E. Cañón-Barriga, Julián D. Giraldo-Ocampo

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Síndrome hepatorrenal en falla hepatica aguda sobre cronica: a proposito de un caso by Christian Camilo Giraldo Ocampo, Maria Fernanda Jiménez Bejarano, Jaime Jose Torres Saltarin

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Case report: Craniofrontonasal syndrome caused by a novel variant in the EFNB1 gene in a Colombian woman by Harry Pachajoa, Harry Pachajoa, Diana Marcela Vasquez-Forero, Diana Marcela Vasquez-Forero, Sebastian Giraldo-Ocampo

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