Showing 1 - 2 results of 2 for search 'Froylan García-Martínez', query time: 0.02s Refine Results
  1. 1
    Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases

    Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases by Vianey Ordoñez-Labastida, Luis Montes-Almanza, Froylan García-Martínez, Juan C. Zenteno

    Published 2022-10-01
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    Article
  2. 2
    Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data‐Based Read‐Depth Approach

    Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data‐Based Read‐Depth Approach by Gerardo E. Fabian‐Morales, Vianey Ordoñez‐Labastida, Froylan Garcia‐Martínez, Luis Montes‐Almanza, Juan C. Zenteno

    Published 2024-10-01
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    Article

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