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Papers published by Dr Diana Ramirez-Montaño:

Original Research

Evaluation of CYP2C19 Gene Polymorphisms in Patients with Acid Peptic Disorders Treated with Esomeprazole

Díaz-Ordóñez L, Ramírez-Montaño D, Candelo E, González-Restrepo C, Silva-Peña S, Rojas CA, Sepulveda Copete M, Echavarria HR, Pachajoa H

Pharmacogenomics and Personalized Medicine 2021, 14:509-520

Published Date: 29 April 2021

Corrigendum

Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype [Corrigendum]

Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D

The Application of Clinical Genetics 2018, 11:75-76

Published Date: 31 May 2018

Case report

Achondrogenesis type 1A: clinical, histologic, molecular, and prenatal ultrasound diagnosis

Vanegas S, Sua LF, López-Tenorio J, Ramírez-Montaño D, Pachajoa H

The Application of Clinical Genetics 2018, 11:69-73

Published Date: 25 May 2018

Case report

Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype

Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D

The Application of Clinical Genetics 2018, 11:15-21

Published Date: 23 March 2018