Showing 1 - 5 results of 5 for search 'Luis Celis', query time: 0.03s Refine Results
  1. 1
    Modulation of thyroid hormone receptor transactivation by the early region 1A (E1A)-like inhibitor of differentiation 1 (EID1)

    Modulation of thyroid hormone receptor transactivation by the early region 1A (E1A)-like inhibitor of differentiation 1 (EID1) by Diana Vargas, Luis Celis, Carolina Romero, Fernando Lizcano

    Published 2008-01-01
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  2. 2
    Progressive Early-Onset Leukodystrophy Related to Biallelic Variants in the <i>KARS</i> Gene: The First Case Described in Latin America

    Progressive Early-Onset Leukodystrophy Related to Biallelic Variants in the <i>KARS</i> Gene: The First Case Described in Latin America by Adriana Vargas, Jorge Rojas, Ivan Aivasovsky, Sergio Vergara, Marianna Castellanos, Carolina Prieto, Luis Celis

    Published 2020-11-01
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  3. 3
    Prenatal Diagnosis of an Unusual Phenotype of Cantrell's Pentalogy: Case Report, and Literature Review

    Prenatal Diagnosis of an Unusual Phenotype of Cantrell's Pentalogy: Case Report, and Literature Review by Ivan Aivasovsky-Trotta, Sergio Vergara-Cardenas, Amenaida Ferrer-Marcano, Lorena Rincones-Rojas, Carolina Prieto-Soler, Ana Bracho-Fernández, Isabel Fernández-González, Luis Celis

    Published 2021-10-01
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  4. 4
    Correlation of the Homeostasis Model Assessment Index and Adiponectin, Leptin and Insulin Levels to Body Mass Index-Associated Gene Polymorphisms in Adolescents

    Correlation of the Homeostasis Model Assessment Index and Adiponectin, Leptin and Insulin Levels to Body Mass Index-Associated Gene Polymorphisms in Adolescents by María D. Martínez-Martínez, Hugo Mendieta-Zerón, Luis Celis, Cristian F. Layton-Tovar, Rocío Torres-García, Laura E. Gutiérrez-Pliego, Eneida Camarillo-Romero, José D. Garduño-García, María D. Camarillo-Romero

    Published 2018-12-01
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  5. 5
    P624: Performance and impact of clinical genome sequencing in patients with suspected rare genetic diseases in Peru

    P624: Performance and impact of clinical genome sequencing in patients with suspected rare genetic diseases in Peru by Erin Thorpe, Milagros Duenas-Roque, Mario Cornejo-Olivas, Jeny Bazalar-Montoya, Nelson Purizaca-Rosillo, Richard Rodriguez, Karina Milla-Neyra, Carlos De La Torre-Hernandez, Elison Sarapura-Castro, Carolina Galarreta Aima, Gioconda Manassero-Morales, Giulliana Chávez-Pasco, Luis Celis-García, Jorge La Serna, Ryan Taft

    Published 2024-01-01
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