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Papers published by Dr Juliana Lores:

Case report

Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies

Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J

Pharmacogenomics and Personalized Medicine 2022, 15:913-918

Published Date: 1 November 2022

Case report

Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1

Perafan-Valdes L, Giraldo-Ocampo S, Lores J, Pachajoa H

Pharmacogenomics and Personalized Medicine 2022, 15:873-878

Published Date: 25 October 2022

Case report

A Novel APOC2 Mutation in a Colombian Patient with Recurrent Hypertriglyceridemic Pancreatitis

Pinilla-Monsalve GD, Lores J, Pachajoa H, López-Ponce de León JD, López A, Rodríguez-Rojas LX, Nastasi-Catanese JA

The Application of Clinical Genetics 2020, 13:63-69

Published Date: 26 March 2020