Novel MYT1 variants expose the complexity of oculo‐auriculo‐vertebral spectrum genetic mechanisms von Zamariolli, Malú, Burssed, Bruna, Moysés‐Oliveira, Mariana, Colovati, Mileny, Bellucco, Fernanda Teixeira da Silva, Santos, Leonardo Caires, Alvarez Perez, Ana Beatriz, Bragagnolo, Silvia, Melaragno, Maria Isabel

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A rare case of trisomy 15pter‐q21.2 due to a de novo marker chromosome von Pacanaro, Ade Nubia Xavier, Christofolini, Denise Maria, Kulikowski, Leslie Domenici, Belangero, Sintia Iole Nogueira, da Silva Bellucco, Fernanda Teixeira, Varela, Monica C., Koiffmann, Celia P., Yoshimoto, Maisa, Squire, Jeremy A., Schiavon, Adriana V., Heck, Benjamin, Melaragno, Maria Isabel

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Trisomy 16q21 → qter: Seven‐year follow‐up of a girl with unusually long survival von de Carvalho, Acácia Fernandes Lacerda, da Silva Bellucco, Fernanda Teixeira, dos Santos, Normeide Pedreira, Pellegrino, Renata, de Azevedo Moreira, Lília Maria, Toralles, Maria Betania Pereira, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel

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Investigating 22q11.2 Deletion and Other Chromosomal Aberrations in Fetuses With Heart Defects Detected by Prenatal Echocardiography von Bellucco, Fernanda Teixeira da Silva, Belangero, Sintia Iole Nogueira, Farah, Leila Montenegro Silveira, Machado, Maria Virgínia Lima, Cruz, Adriano Pastor, Lopes, Lílian Maria, Lopes, Marco Antonio Borges, Zugaib, Marcelo, Cernach, Mirlene Cecília, Melaragno, Maria Isabel

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Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation von de Carvalho, Acácia Fernandes Lacerda, da Silva Bellucco, Fernanda Teixeira, Kulikowski, Leslie Domenici, Toralles, Maria Betânia Pereira, Melaragno, Maria Isabel

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Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation von Kulikowski, Leslie Domenici, Yoshimoto, Maisa, Teixeira da Silva Bellucco, Fernanda, Nogueira Belangero, Sintia Iole, Christofolini, Denise Maria, Xavier Pacanaro, Ade Nubia, Bortolai, Adriana, de Arruda Cardoso Smith, Marilia, Squire, Jeremy A, Melaragno, Maria Isabel

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Interrupted aortic arch type B in A patient with cat eye syndrome von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda Teixeira da Silva, Cernach, Mirlene C S P, Hacker, April M, Emanuel, Beverly S, Melaragno, Maria Isabel

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Partial 5p monosomy or trisomy in 11 patients from a family with a t von de Carvalho, Acácia Fernandes Lacerda, da Silva Bellucco, Fernanda Teixeira, Kulikowski, Leslie Domenici, Toralles, Maria Betânia Pereira, Melaragno, Maria Isabel

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Trisomy 16q21 right arrow qter: Seven-year follow-up of a girl with unusually long survival von De Carvalho, Acacia Fernandes Lacerda, Da Silva Bellucco, Fernanda Teixeira, Dos Santos, Normeide Pedreira, Pellegrino, Renata, De Azevedo Moreira, Lilia Maria, Toralles, Maria Betania Pereira, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel

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Interrupção do arco aórtico tipo B em uma paciente com síndrome de olho de gato von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda Teixeira da Silva, Cernach, Mirlene C. S. P., Hacker, April M., Emanuel, Beverly S., Melaragno, Maria Isabel

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Interrupção do arco aórtico tipo B em uma paciente com síndrome de olho de gato von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda Teixeira da Silva, Cernach, Mirlene C. S. P., Hacker, April M., Emanuel, Beverly S., Melaragno, Maria Isabel

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Interrupção do arco aórtico tipo B em uma paciente com síndrome de olho de gato Interrupción del arco aórtico tipo B en una paciente con síndrome del ojo de gato Interrupted aortic... von Sintia Iole Nogueira Belangero, Fernanda Teixeira da Silva Bellucco, Mirlene C. S. P. Cernach, April M. Hacker, Beverly S. Emanuel, Maria Isabel Melaragno

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Trisomy 16q21 → qter: Seven-year follow-up of a girl with unusually long survival von de Carvalho, Acácia Fernandes Lacerda, da Silva Bellucco, Fernanda Teixeira, dos Santos, Normeide Pedreira, Pellegrino, Renata, de Azevedo Moreira, Lília Maria, Toralles, Maria Betania Pereira, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel

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A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome von Pacanaro, Ade Nubia Xavier, Christofolini, Denise Maria, Kulikowski, Leslie Domenici, Belangero, Sintia Iole Nogueira, da Silva Bellucco, Fernanda Teixeira, Varela, Monica C., Koiffmann, Celia P., Yoshimoto, Maisa, Squire, Jeremy A., Schiavon, Adriana V., Heck, Benjamin, Melaragno, Maria Isabel

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Post-mortem cytogenomic investigations in patients with congenital malformations von Dias, Alexandre Torchio, Zanardo, Évelin Aline, Dutra, Roberta Lelis, Piazzon, Flavia Balbo, Novo-Filho, Gil Monteiro, Montenegro, Marilia Moreira, Nascimento, Amom Mendes, Rocha, Mariana, Madia, Fabricia Andreia Rosa, Costa, Thais Virgínia Moura Machado, Milani, Cintia, Schultz, Regina, Gonçalves, Fernanda Toledo, Fridman, Cintia, Yamamoto, Guilherme Lopes, Bertola, Débora Romeo, Kim, Chong Ae, Kulikowski, Leslie Domenici

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