A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) by Romero, V. I., Pozo, J. C., Saenz, S., Llamos-Paneque, A., Liehr, T., Hosomichi, K., Tajima, A.

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A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) by Romero, V I, Pozo, J C, Saenz, S, Llamos-Paneque, A, Liehr, T, Hosomichi, K, Tajima, A

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Experiences of the Molecular Diagnosis of Fragile X Syndrome in Ecuador by Pozo-Palacios, Juan, Llamos-Paneque, Arianne, Rivas, Christian, Onofre, Emily, López-Cáceres, Andrea, Villareal, Jenniffer

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Rubinstein–Taybi syndrome in diverse populations by Tekendo‐Ngongang, Cedrik, Owosela, Babajide, Fleischer, Nicole, Addissie, Yonit A., Malonga, Bryan, Badoe, Ebenezer, Gupta, Neerja, Moresco, Angélica, Huckstadt, Victoria, Ashaat, Engy A., Hussen, Dalia Farouk, Luk, Ho‐Ming, Lo, Ivan F. M., Hon‐Yin Chung, Brian, Fung, Jasmine L. F., Moretti‐Ferreira, Danilo, Batista, Letícia Cassimiro, Lotz‐Esquivel, Stephanie, Saborio‐Rocafort, Manuel, Badilla‐Porras, Ramses, Penon Portmann, Monica, Jones, Kelly L., Abdul‐Rahman, Omar A., Uwineza, Annette, Prijoles, Eloise J., Ifeorah, Ifeanyi Kanayo, Llamos Paneque, Arianne, Sirisena, Nirmala D., Dowsett, Leah, Lee, Sansan, Cappuccio, Gerarda, Kitchin, Carolyn Sian, Diaz‐Kuan, Alicia, Thong, Meow‐Keong, Obregon, María Gabriela, Mutesa, Leon, Dissanayake, Vajira H. W., El Ruby, Mona O., Brunetti‐Pierri, Nicola, Ekure, Ekanem Nsikak, Stevenson, Roger E., Muenke, Maximilian, Kruszka, Paul

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Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology by Elouej, Sahar, Harhouri, Karim, Mao, Morgane Le, Baujat, Genevieve, Nampoothiri, Sheela, Kayserili, Hϋlya, Menabawy, Nihal Al, Selim, Laila, Paneque, Arianne Llamos, Kubisch, Christian, Lessel, Davor, Rubinsztajn, Robert, Charar, Chayki, Bartoli, Catherine, Airault, Coraline, Deleuze, Jean-François, Rötig, Agnes, Bauer, Peter, Pereira, Catarina, Loh, Abigail, Escande-Beillard, Nathalie, Muchir, Antoine, Martino, Lisa, Gruenbaum, Yosef, Lee, Song-Hua, Manivet, Philippe, Lenaers, Guy, Reversade, Bruno, Lévy, Nicolas, De Sandre-Giovannoli, Annachiara

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Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphisms by Paz‐y‐Miño, César, Yumiceba, Verónica, Moreta, Germania, Paredes, Rosario, Ruiz, Mónica, Ocampo, Ligia, Llamos Paneque, Arianne, Ochoa Pérez, Catalina, Ruiz‐Cabezas, Juan Carlos, Álvarez Vidal, Jenny, Jiménez Torres, Idarmis, Vargas‐Vera, Ramón, Cruz, Fernando, Guapi N, Víctor Hugo, Montalván, Martha, Meneses Álvarez, Sara, Garzón Castro, Maribel, Lamar Segura, Elizabeth, Recalde Báez, María Augusta, Naranjo, María Elena, Tambaco Jijón, Nina, Sinche, María, Licuy, Pedro, Burgos, Ramiro, Porras‐Borja, Fabián, Echeverría‐Garcés, Gabriela, Pérez‐Villa, Andy, Armendáriz‐Castillo, Isaac, García‐Cárdenas, Jennyfer M., Guerrero, Santiago, Guevara‐Ramírez, Patricia, López‐Cortés, Andrés, Zambrano, Ana Karina, Leone, Paola E.

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Novel EYA1 Variants Causing Branchio-Oto-Renal Syndrome by Klingbeil, Kyle D, Greenland, Christopher M, Arslan, Selcuk, Llamos Paneque, Arianne, Gurkan, Hakan, Demir Ulusal, Selma, Maroofian, Reza, Carrera-Gonzalez, Andrea, Montufar-Armendariz, Stefany, Paredes, Rosario, Elcioglu, Nursel, Menendez, Ibis, Behnam, Mahdiyeh, Foster, Joseph, Guo, Shengru, Escarfuller, Sebastian, Cengiz, Filiz Basak, Duman, Duygu, Bademci, Guney, Tekin, Mustafa

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Turner syndrome associated with Down syndrome: about a case by Llamos-Paneque, Arianne, Pozo-Palacios, Juan C., Sancan-Jalca, Byron, Garzón-Castro, Maribel, Lamar-Segura, Elizabeth, Óacato-Pachacama, Karen L., Tiehr, Thomas L.

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Variantes citogenéticas en pacientes con síndrome de Turner diagnosticadas en un hospital de tercer nivel de atención en Ecuador by Llamos-Paneque, Arianne, Óacato, Karen L., Lamar-Segura, Elizabeth, Garzón-Castro, Maribel, Recalde-Báez, María A., Román-Naranjo, María E., Vásquez, Gabriel

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Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology by Elouej, Sahar, Harhouri, Karim, Le Mao, Morgane, Baujat, Genevieve, Nampoothiri, Sheela, Kayserili, Hϋlya, Menabawy, Nihal Al, Selim, Laila, Paneque, Arianne Llamos, Kubisch, Christian, Lessel, Davor, Rubinsztajn, Robert, Charar, Chayki, Bartoli, Catherine, Airault, Coraline, Deleuze, Jean-François, Rötig, Agnes, Bauer, Peter, Pereira, Catarina, Loh, Abigail, Escande-Beillard, Nathalie, Muchir, Antoine, Martino, Lisa, Gruenbaum, Yosef, Lee, Song-Hua, Manivet, Philippe, Lenaers, Guy, Reversade, Bruno, Lévy, Nicolas, De Sandre-Giovannoli, Annachiara

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Varones 46, XX: a propósito de dos casos genéticamente distintos by Paneque, Arianne Llamos, Armendáriz, Stefany Montúfar, Reyes Silva, Carlos Alberto, Garzón Castro, Maribel de los Ángeles, Tambaco Jijón, Nina Jacinta

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