CGH analysis in Colombian patients: findings of 1374 arrays in a seven-year study von García-Acero, Mary, Suárez-Obando, Fernando, Gómez-Gutiérrez, Alberto

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Identification of common differentially expressed genes in Turner (45,X) and Klinefelter (47,XXY) syndromes using bioinformatics analysis von Manotas, María Carolina, Calderón, Juan Camilo, López-Kleine, Liliana, Suárez-Obando, Fernando, Moreno, Olga M., Rojas, Adriana

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Novel homozygous mutation in a colombian patient with persistent müllerian duct syndrome: expanded phenotype von Acero, Mary García, Moreno, Olga, Gutiérrez, Andrés, Sánchez, Catalina, Cataño, Juan Guillermo, Suárez-Obando, Fernando, Rojas, Adriana

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An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review) von Moreno, Olga Maria, Paredes, Angela Camila, Suarez-Obando, Fernando, Rojas, Adriana

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Epigenetic mechanisms and host factors impact ACE2 gene expression: Implications in COVID-19 susceptibility von Daniel, González, Paola, Ayala-Ramírez, Nancy, Gelvez, Fernando, Suarez-Obando, Beatriz, Ariza, Zulema, Ruiz, Julieth, Arcila, Claudia, Cardozo, Adriana, Rojas

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P-19 ASSOCIATION OF TM6SF2 GENE POLYMORPHISMS WITH CARDIOVASCULAR RISK IN PATIENTS WITH METABOLIC DYSFUNCTION–ASSOCIATED STEATOTIC LIVER DISEASE (MASLD) IN A HISPANIC ADULT POPULAT... von CUERVO, LUISA FERNANDA SANTOS, Santamaria, Maria Claudia Noguera, Trujillo, Carlos Andres Ortiz, Obando, Fernando Suarez, Puerta, Adriana Varon

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Implementing Technology-Supported Care for Depression and Alcohol Use Disorder in Primary Care in Colombia: Preliminary Findings von Torrey, William C, Cepeda, Magda, Castro, Sergio, Bartels, Sophia M, Cubillos, Leonardo, Obando, Fernando Suárez, Camblor, Pablo Martínez, Uribe-Restrepo, José Miguel, Williams, Makeda, Gómez-Restrepo, Carlos, Marsch, Lisa A

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Integrating Depression and Alcohol Use Care Into Primary Care in Low- and Middle-Income Countries: A Meta-Analysis von Park, Sena, Cubillos, Leonardo, Martinez-Camblor, Pablo, Bartels, Sophia M, Torrey, William C, John, Deepak T, Cepeda, Magda, Bell, Kathleen, Castro, Sergio, Suárez-Obando, Fernando, Uribe-Restrepo, José Miguel, Gómez-Restrepo, Carlos, Marsch, Lisa A

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Urea Cycle Defects: Early-Onset Disease Associated with A208T Mutation in OTC Gene—Expanding the Clinical Phenotype von Suárez-Obando, Fernando, García, Mary, Rincon, Alejandra, Sánchez, Ana Isabel

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Scaling Up Science-Based Care for Depression and Unhealthy Alcohol Use in Colombia: An Implementation Science Project von Marsch, Lisa A, Gómez-Restrepo, Carlos, Bartels, Sophie M, Bell, Kathleen, Camblor, Pablo Martinez, Castro, Sergio, Cárdenas Charry, Maria Paula, Cepeda, Magda, Cubillos, Leonardo, John, Deepak, Jassir, Maria Paula, Lemley, Shea M, Suárez-Obando, Fernando, Torrey, William C, Uribe, José Miguel, Williams, Makeda J

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Gene dosage of DAX-1, determining in sexual differentiation: duplication of DAX-1 in two sisters with gonadal dysgenesis von García-Acero, Mary, Molina, Mónica, Moreno, Olga, Ramirez, Andrea, Forero, Catalina, Céspedes, Camila, Prieto, Juan Carlos, Pérez, Jaime, Suárez-Obando, Fernando, Rojas, Adriana

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The benefits and challenges of family genetic testing in rare genetic diseases—lessons from Fabry disease von Germain, Dominique P., Moiseev, Sergey, Suárez‐Obando, Fernando, Al Ismaili, Faisal, Al Khawaja, Huda, Altarescu, Gheona, Barreto, Fellype C., Haddoum, Farid, Hadipour, Fatemeh, Maksimova, Irina, Kramis, Mirelle, Nampoothiri, Sheela, Nguyen, Khanh Ngoc, Niu, Dau‐Ming, Politei, Juan, Ro, Long‐Sun, Vu Chi, Dung, Chen, Nan, Kutsev, Sergey

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Epigenetic control of SOX9 gene by the histone acetyltransferase P300 in human Sertoli cells von González, Daniel, Peña, María José, Bernal, Camila, García-Acero, Mary, Manotas, Maria Carolina, Suarez-Obando, Fernando, Rojas, Adriana

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Disorders of sex development: Genetic characterization of a patient cohort von García-Acero, Mary, Moreno-Niño, Olga, Suárez-Obando, Fernando, Molina, Mónica, Manotas, María Carolina, Prieto, Juan Carlos, Forero, Catalina, Céspedes, Camila, Pérez, Jaime, Fernandez, Nicolas, Rojas, Adriana

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Variants in the Sequence of the Probe Hybridization Site May Affect MLPA Performance in Patients with Duchenne/Becker Muscular Dystrophy von Buitrago, Tatiana, García-Acero, Mary, Guerra-Torres, Mariana, Pineda, Tatiana, Gámez, Tatiana, Suárez-Obando, Fernando, García-Robles, Reggie, Ayala-Ramírez, Paola

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Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review von Suarez-Obando, Fernando, Ortiz-Corredor, Fernando, Correa-Arrieta, Cristian, Quiroga-Carrillo, Manuela

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Detection of hearing loss in newborns: Definition of a screening strategy in Bogotá, Colombia von Olarte, Margarita, Bermúdez Rey, María Carolina, Beltran, Angela P., Guerrero, Diana, Suárez-Obando, Fernando, López, Greizy, García, Mary, Ospina, Juan C., Fonseca, Carol, Bertolotto, Ana M., Aldana, Nubia, Gelvez, Nancy, Tamayo, Martha L.

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Clinical and Molecular Cytogenetic Characteristics of Five Cases with Isodicentric Y Chromosome von Manotas, María C., García-Acero, Mary, González, Daniel M., Moreno, Olga M., Suárez-Obando, Fernando, Céspedes, Camila, Forero, Catalina, Pérez, Jaime, Fernández, Nicolás, Rojas, Adriana

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Perceived access to general and mental healthcare in primary care in Colombia during COVID-19: A cross-sectional study von Gómez-Restrepo, Carlos, Cepeda, Magda, Torrey, William C, Suarez-Obando, Fernando, Uribe-Restrepo, José Miguel, Park, Sena, Acosta, María Paula Jassir, Camblor, Pablo Martínez, Castro, Sergio M, Aguilera-Cruz, Jeny, González, Lilian, Chaparro, Natalia, Gómez-Gamez, Ana María, Bell, Kathleen, Marsch, Lisa A

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The clinical profiles of female patients with Fabry disease in Latin America: A Fabry Registry analysis of natural history data from 169 patients based on enzyme replacement therap... von Martins, Ana M., Cabrera, Gustavo, Molt, Fernando, Suárez‐Obando, Fernando, Valdés, Régulo A., Varas, Carmen, Yang, Meng, Politei, Juan M.

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