Showing 1 - 4 results of 4 for search 'Díaz-Ordoñez L', query time: 0.03s Refine Results
  1. 1
    A Novel Intronic KMT2D Variant as a Cause of Kabuki Syndrome: A Case Report

    A Novel Intronic KMT2D Variant as a Cause of Kabuki Syndrome: A Case Report by Aristizábal E, Diaz-Ordóñez L, Candelo E, Pachajoa H

    Published 2021-10-01
    Get full text
    Article
  2. 2
    A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome

    A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome by Ríos-Serna LJ, Díaz-Ordoñez L, Candelo E, Pachajoa H

    Published 2018-11-01
    Get full text
    Article
  3. 3
    Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations

    Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations by Ciro Acosta S, Díaz-Ordóñez L, Gutierrez-Medina JD, Silva-Cuero YK, Arango-Vélez LG, García-Trujillo AO, Pachajoa H

    Published 2024-02-01
    Get full text
    Article
  4. 4
    Evaluation of CYP2C19 Gene Polymorphisms in Patients with Acid Peptic Disorders Treated with Esomeprazole

    Evaluation of CYP2C19 Gene Polymorphisms in Patients with Acid Peptic Disorders Treated with Esomeprazole by Díaz-Ordóñez L, Ramírez-Montaño D, Candelo E, González-Restrepo C, Silva-Peña S, Rojas CA, Sepulveda Copete M, Echavarria HR, Pachajoa H

    Published 2021-04-01
    Get full text
    Article

Search Tools: