Search Results - Chacon‐Camacho, Oscar Francisco

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    Review and update on the molecular basis of Leber congenital amaurosis

    Review and update on the molecular basis of Leber congenital amaurosis by Chacon-Camacho, Oscar Francisco, Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    TEK gene‐related primary congenital glaucoma: Phenotypic features and mutational spectrum in a Mexican cohort of 10 unrelated families

    TEK gene‐related primary congenital glaucoma: Phenotypic features and mutational spectrum in a Mexican cohort of 10 unrelated families by Chacon‐Camacho, Oscar Francisco, Ordaz‐Robles, Thania, Cid‐García, Marion Aline, Hofmann‐Blancas, María Enriqueta, Ledesma‐Gil, Jasbeth, García‐Huerta, María Magdalena, Prado‐Larrea, Carolina, Cortés‐González, Vianney, Lozano‐Garza, Rodrigo Isaac, García‐Vega, Daphne, Kim, JiHye, Khang, Rin, Lee, Eugene, Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  3. 3
    TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes

    TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes by Chacon-Camacho, Oscar Francisco, Fuerte-Flores, Bertha Irene, Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    SOX2 anophthalmia syndrome and dental anomalies

    SOX2 anophthalmia syndrome and dental anomalies by Chacon-Camacho, Oscar Francisco, Fuerte-Flores, Bertha Irene, Ricardez-Marcial, Edgar F., Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  5. 5
    A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers

    A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers by Arce-González, Rocío, Chacon-Camacho, Oscar Francisco, Ordoñez-Labastida, Vianey, Graue-Hernandez, Enrique O., Navas-Pérez, Alejandro, Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population

    Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population by Macriz-Romero, Nicole, Vera-Duarte, Guillermo Raul, Guerrero-Becerril, Jesus, Chacón-Camacho, Oscar Francisco, Astiazarán, Mirena C, Zenteno, Juan Carlos, Graue-Hernandez, Enrique O.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  7. 7
    A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy

    A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy by Piña-Aguilar, Raul Eduardo, Regalado-Hernández, Miguel Ángel, Moreno-García, Jesús Daniel, Buentello-Volante, Beatriz, Chacón-Camacho, Oscar Francisco, Gallegos-Rivas, Mayra Celina, Kazakova, Ekaterina, Santillán-Hernández, Yuritzi, Zenteno, Juan Carlos

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  8. 8
    TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes

    TP63 mutation in a patient with acro-dermo-ungual-lacrimal-tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes by Chacon-Camacho, Oscar Francisco, Fuerte-Flores, Bertha Irene, Zenteno, Juan Carlos

    Get full text
    Report
    Save to List
    Saved in:
  9. 9
    A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy

    A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy by Piña-Aguilar, Raul Eduardo, Regalado-Hernández, Miguel Ángel, Moreno-García, Jesús Daniel, Buentello-Volante, Beatriz, Chacón-Camacho, Oscar Francisco, Gallegos-Rivas, Mayra Celina, Kazakova, Ekaterina, Santillán-Hernández, Yuritzi, Zenteno, Juan Carlos

    Get full text
    Report
    Save to List
    Saved in:

Search Tools: