Telomere shortening in late‐life depression: A potential marker of depression severity von Mendes‐Silva, Ana Paula, Vieira, Erica Leandro Marciano, Xavier, Gabriela, Barroso, Lucelia Scarabeli Silva, Bertola, Laiss, Martins, Efrem Augusto Ribeiro, Brietzke, Elisa Macedo, Belangero, Sintia Iole Nogueira, Diniz, Breno Satler

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Is there an association between cortical thickness, age of onset, and duration of illness in schizophrenia? von Assunção Leme, Idaiane Batista, Gadelha, Ary, Sato, João Ricardo, Kiyomi Ota, Vanessa, de Jesus Mari, Jair, Melaragno, Maria Isabel, de Arruda Cardoso Smith, Marilia, Nogueira Belangero, Sintia Iole, Bressan, Rodrigo Affonseca, Jackowski, Andrea Parolin

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Male infertility related to an aberrant karyotype, 46,XY,9ph,9qh von Belangero, Síntia Iole Nogueira, Ph.D, Christofolini, Denise Maria, M.S, Bianco, Bianca, M.S, Gava, Marcello Machado, M.D, Wroclawski, Eric Roger, M.D, Barbosa, Caio Parente, M.D., Ph.D

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Effects of the brain-derived neurotropic factor variant Val66Met on cortical structure in late childhood and early adolescence von de Araujo, Celia Maria, Zugman, Andre, Swardfager, Walter, Belangero, Sintia Iole Nogueira, Ota, Vanessa Kiyomi, Spindola, Leticia Maria, Hakonarson, Hakon, Pellegrino, Renata, Gadelha, Ary, Salum, Giovanni Abrahão, Pan, Pedro Mario, de Moura, Luciana Monteiro, Del Aquilla, Marco, Picon, Felipe Almeida, Amaro, Edson, Sato, João Ricardo, Brietzke, Elisa, Grassi-Oliveira, Rodrigo, Rohde, Luis Augusto P., Miguel, Euripedes Constantino, Bressan, Rodrigo A., Jackowski, Andrea Parolin

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Expression Profile of Collagen Genes in Shoulder Instability von Belangero, Paulo Santoro, MD, Brazil, Leal, Mariana Ferreira, PhD, Brazil, Machado, Gabriel Esquitini, Brazil, De Figueiredo, Eduardo Antonio, MD, Brazil, Andreoli, Carlos Vicente, Brazil, Cohen, Carina, MD, Brazil, Terra, Bernardo Barcellos, MD, Brazil, Monteiro, Gustavo Cara, MD, Brazil, Pochini, Alberto Castro, MD, Brazil, Belangero, Sintia Iole Nogueira, PhD, Brazil, Ejnisman, Benno, MD, Brazil, Cohen, Moises, MD, PhD, Brazil

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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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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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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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Stress-related telomere length in children: A systematic review von Coimbra, Bruno Messina, Carvalho, Carolina Muniz, Moretti, Patricia Natalia, de Mello, Marcelo Feijó, Belangero, Sintia Iole Nogueira

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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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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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Deleção 22q11.2 em pacientes com defeito cardíaco conotruncal e fenótipo da síndrome da deleção 22q11.2 von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda T.S., Kulikowski, Leslie Domenici, Christofolini, Denise M., Cernach, Mirlene C. S. P., Melaragno, Maria Isabel

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22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda T S, Kulikowski, Leslie Domenici, Christofolini, Denise M, Cernach, Mirlene C S P, Melaragno, Maria Isabel

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Deleção 22q11.2 em pacientes com defeito cardíaco conotruncal e fenótipo da síndrome da deleção 22q11.2 Deleción 22q11.2 en pacientes con defecto cardiaco conotruncal y fenotipo de... von Sintia Iole Nogueira Belangero, Fernanda T.S. Bellucco, Leslie Domenici Kulikowski, Denise M. Christofolini, Mirlene C. S. P. Cernach, Maria Isabel Melaragno

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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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Deleção 22q11.2 em pacientes com defeito cardíaco conotruncal e fenótipo da síndrome da deleção 22q11.2 von Belangero, Sintia Iole Nogueira, Bellucco, Fernanda T.S., Kulikowski, Leslie Domenici, Christofolini, Denise M., Cernach, Mirlene C. S. P., 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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