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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Electrostimulation to Increase Peroneal Muscle Strength in Pediatric Patients With Postsurgical Clubfoot von Morales-Osorio, Guadalupe, Lomeli-Gonzalez, Joel, Hernandez-Valadez, Noemi Isela, Saldana, Elena Arellano, Arenas-Sordo, Maria Luz

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Global Developmental Delay in a Mexican Patient With Megalencephalic Leukoencephalopathy With Subcortical Cysts von Cerecedo Zapata, Cesar Misael, Villafuerte De la Cruz, Rocio Adriana, Cortes Rubio, Ana Maria, Kramis Hollands, Mirelle, Flores Estrada, Ivonne Natalia, Luz Arenas Sordo, Maria

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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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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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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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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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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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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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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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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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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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Electrostimulation to Increase Peroneal Muscle Strength in Pediatric Patients With Postsurgical Clubfoot von Guadalupe Morales-Osorio, Joel Lomeli-Gonzalez, Noemi Isela Hernandez-Valadez, Elena Arellano Saldana, Maria Luz Arenas-Sordo

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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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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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Global Developmental Delay in a Mexican Patient With Megalencephalic Leukoencephalopathy With Subcortical Cysts von Cesar Misael Cerecedo Zapata, Rocio Adriana Villafuerte De la Cruz, Ana Maria Cortes Rubio, Mirelle Kramis Hollands, Ivonne Natalia Flores Estrada, Maria Luz Arenas Sordo

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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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