Search Results - Giraldo-Ocampo S

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

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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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2q31 microdeletion syndrome with the velocardiofacial phenotype and review of the literature: a case report by Estephania Candelo, Sebastian Giraldo-Ocampo, Julian Nevado, Pablo Lapunzina, Harry Pachajoa

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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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