Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment von Bahena, Paulina, Daftarian, Narsis, Maroofian, Reza, Linares, Paola, Villalobos, Daniel, Mirrahimi, Mehraban, Rad, Aboulfazl, Doll, Julia, Hofrichter, Michaela A. H., Koparir, Asuman, Röder, Tabea, Han, Seungbin, Sabbaghi, Hamideh, Ahmadieh, Hamid, Behboudi, Hassan, Villanueva-Mendoza, Cristina, Cortés-Gonzalez, Vianney, Zamora-Ortiz, Rocio, Kohl, Susanne, Kuehlewein, Laura, Darvish, Hossein, Alehabib, Elham, Arenas-Sordo, Maria de la Luz, Suri, Fatemeh, Vona, Barbara, Haaf, Thomas

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Developmental Coordination Disorder: Comparison Between 2 Therapeutic Models von Avalos-Robles, Karla F, Viñals-Labañino, Carlos P, Arellano-Saldaña, Elena, Arenas-Sordo, María de la Luz

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PPARG-LYPLAL1 Multi-Allelic Combination Associated with Obesity and Overweight in Mexican Adolescent Females von Hernández-Tobías, Esther Alhelí, Torres-Sánchez, Luisa, Noris, Gino, Santana, Carla, Samano, María Reyna, Arellano-Galindo, José, de la Luz Arenas-Sordo, María, Brooks, Daniel, Rodríguez-Ventura, Ana Lilia, Meraz-Ríos, Marco Antonio, Gómez, Rocío

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Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort von Cengiz, Filiz Basak, Yilmazer, Rasim, Olgun, Levent, Sennaroglu, Levent, Kirazli, Tayfun, Alper, Hudaver, Olgun, Yuksel, Incesulu, Armagan, Atik, Tahir, Huesca-Hernandez, Fabiola, Domínguez-Aburto, Juan, González-Rosado, Garly, Hernandez-Zamora, Edgar, Arenas-Sordo, Maria de la Luz, Menendez, Ibis, Orhan, Kadir Serkan, Avci, Hakan, Mahdieh, Nejat, Bonyadi, Mortaza, Foster, Joseph, Duman, Duygu, Ozkinay, Ferda, Blanton, Susan H., Bademci, Guney, Tekin, Mustafa

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Sordera neurosensorial congénita con malformación de oído interno ligada al X en una familia mexicana von Huesca-Hernández, Fabiola, Domínguez-Aburto, Juan, Aguilera-Tello, Silvia Alejandra, Arenas-Sordo, María de la Luz, González-Rosado, Garly

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ALOX5 , LPA , MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans von Camacho-Mejorado, Rafael, Gómez, Rocío, Torres-Sánchez, Luisa E, Alhelí Hernández-Tobías, Esther, Noris, Gino, Santana, Carla, Magaña, Jonathan J, Orozco, Lorena, de la Peña-Díaz, Aurora, de la Luz Arenas-Sordo, María, Meraz-Ríos, Marco Antonio, Majluf-Cruz, Abraham

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Correction to ' ALOX5, LPA, MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans' von Camacho-Mejorado, Rafael, Gómez, Rocío, Torres-Sánchez, Luisa E, Alhelí Hernández-Tobías, Esther, Noris, Gino, Santana, Carla, Magaña, Jonathan J, Orozco, Lorena, de la Peña-Díaz, Aurora, de la Luz Arenas-Sordo, María, Antonio Meraz-Ríos, Marco, Majluf-Cruz, Abraham

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Capillary electrophoresis for the detection of PMP22 gene duplication: Study in Mexican patients von Hernández-Zamora, Edgar, de la Luz Arenas-Sordo, María, Maldonado-Rodríguez, Rogelio

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Leiden V factor and spastic cerebral palsy in Mexican children von Arenas-Sordo, María de la Luz, Zavala-Hernández, César, Casiano-Rosas, César, Reyes-Maldonado, Elba, Ríos, Camilo, Hernández-Zamora, Edgar, Del Valle-Cabrera, Martha G, Yamamoto-Furusho, Jesús K

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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort von Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Diaz-Horta, Oscar, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Huesca-Hernandez, Fabiola, de la Luz Arenas-Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza-Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen-Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa

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La electroforesis capilar como una nueva estrategia en la medicina y el diagnóstico clínico von Jonathan J Magaña, María de la Luz Arenas-Sordo, Rocío Gómez

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Microarray design using virtual hybridization to study variations in REP-CMT1A sites von Hernández-Zamora, Edgar, Arenas-Sordo, María de la Luz, Maldonado-Rodríguez, Rogelio

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Sordera neurosensorial congénita con malformación de oído interno ligada al X en una familia mexicana von Arenas Sordo, María de la Luz, Domínguez Aburto, Juan, González Rosado, Garly, Aguilera Tello, Silvia A, Huesca Hernández, Fabiola

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Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants von Hamilton, Eline M.C, Tekturk, Pinar, Cialdella, Fia, van Rappard, Diane F, Wolf, Nicole I, Yalcinkaya, Cengiz, Çetinçelik, Ümran, Rajaee, Ahmad, Kariminejad, Ariana, Paprocka, Justyna, Yapici, Zuhal, Bošnjak, Vlatka Mejaški, van der Knaap, Marjo S

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Translation, cross-cultural adaptation and validation of the General Movement checklist von Salazar-Díaz, Daniela Eugenia, Viñals-Labañino, Carlos P, Balderas-Campos, Marcela, Alvarado-Solorio, Elsa, de la Luz Arenas-Sordo, María

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Strategies for clinical and molecular diagnosis of Charcot-Marie-Tooth 1A among Mexican patients von Hernández-Zamora, Edgar, Arenas-Sordo, Maria de la Luz, Escobar-Cedillo, Rosa Elena, González-Huerta, Norma Celia, Leyva-García, Norberto, Maldonado-Rodríguez, Rogelio

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Síndrome de Cockayne: Informe de un caso: revisión de la literatura von Arenas Sordo, María de la Luz, Hernández Zamora, Edgar, Montoya Pérez, Luis A, Aldape Barrios, B

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Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort von Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Horta, Oscar Diaz, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Hernandez, Fabiola Huesca, de la Luz Arenas Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa

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Unique spectrum of GJB2 mutations in Mexico von de la Luz Arenas-Sordo, Maria, Menendez, Ibis, Hernández-Zamora, Edgar, Sirmaci, Asli, Gutiérrez-Tinajero, Diana, McGetrick, Molly, Murphy-Ruiz, Paulina, Leyva-Juárez, Xolotl, Huesca-Hernández, Fabiola, Dominguez-Aburto, Juan, Tekin, Mustafa

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Capillary electrophoresis, a new diagnostic tool von Magaña, Jonathan J, de la Luz Arenas-Sordo, María, Gómez Ortega, Rocío

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