Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system von Pires, Sílvia, Jorge, Paula, Liehr, Thomas, Oliva-Teles, Natália

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Brain Calcifications in Complex Sexual Aneuploidy von Oliveira, Vanessa, Pedro Rocha, José, Candeias, Cristina, Oliva‐Teles, Natália, Damásio, Joana

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Subtelomeric Rearrangements: Presentation of 21 Probands with Emphasis on Familial Cases von Soares, Ana Rita, Soares, Gabriela, Mota-Freitas, Manuela, Oliva-Teles, Natália, Fortuna, Ana Maria

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Partial tetrasomy 18 mosaicism: Pre and postnatal diagnosis of a unique pattern von Luís, Telma, Candeias, Cristina, Domingues, Sara, Oliva-Teles, Natália, Mota, Céu, Reis, Cláudia Falcão

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20 years of the ICRC Code of Conduct for Disaster Relief: what do we need to improve? von Borovecki, Ana, Einarsdóttir, Jónína, O'Mathúna, Dónal, Pospieszna, Paulina, Stern, Orly Maya, Teles, Natália Oliva

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Blueberry Muffin Syndrome and Hyperleukocytosis in a Newborn: A Diagnostic Challenge von Teixeira, Beatriz, Losa, Ana, Meireles, Andreia, Lachado, Ana, Couto Guerra, Isabel, Machado, Susana, Branco, Lídia, Paulino, Paulo, Lau, Catarina, Oliva-Teles, Natália, Mendes, Carlos, Oliva, Tereza, Pinho, Liliana, Neiva, Luísa, Proença, Elisa

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Ambiguous Genitalia: An Unexpected Diagnosis in a Newborn von Losa, Ana, Da Silva Cardoso, Juliana, Leite, Sara, Barros, Ana Cristina, Guedes, Ana, Rodrigues, Cidade, Borges, Teresa, Oliva-Teles, Natália, Soares, Ana Rita, Mota, Céu

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A Novel Frameshift CHD4 Variant Leading to Sifrim-Hitz-Weiss Syndrome in a Proband with a Subclinical Familial t(17;19) and a Large dup(2)(q14.3q21.1) von Da Silva, Jorge Diogo, Oliva-Teles, Natália, Tkachenko, Nataliya, Fino, Joana, Marques, Mariana, Fortuna, Ana Maria, David, Dezso

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Diagnóstico genético pré-implantação: aspetos técnicos e considerações éticas von Oliva Teles, Natália

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The sense of responsibility in the context of professional activities in Medical Genetics von Oliva-Teles, Natália

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Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature von Oliva-Teles, Natália, de Stefano, Maria Chiara, Gallagher, Louise, Rakic, Severin, Jorge, Paula, Cuturilo, Goran, Markovska-Simoska, Silvana, Borg, Isabella, Wolstencroft, Jeanne, Tümer, Zeynep, Harwood, Adrian J, Kodra, Yllka, Skuse, David

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Lifting the Burden of Sudden Cardiac Arrest Through International Collaboration von Oliva-Teles, Natália, Baldi, Enrico, Böttiger, Bernd W., Empana, Jean-Philippe, Jonsson, Martin, Ristagno, Giuseppe, Tfelt-Hansen, Jacob, Tan, Hanno L.

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Lifting the Burden of Sudden Cardiac Arrest Through International Collaboration: The PARQ Project (EU-COST Action) von Oliva-Teles, Natália, Baldi, Enrico, Böttiger, Bernd W., Empana, Jean-Philippe, Jonsson, Martin, Ristagno, Giuseppe, Tfelt-Hansen, Jacob, Tan, Hanno L.

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Avaliação do conhecimento dos anestesiologistas sobre cuidados paliativos von Santos, Maria de Fátima Oliveira dos, Teles, Natália Oliva, Oliveira, Harison José de, Gomes, Nicole de Castro, Tavares, Joana Cariri Valkasser, Nóbrega, Edilza Câmara

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Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium von Chawner, Samuel J.R.A., Mihaljevic, Marina, Morrison, Sinead, Eser, Hale Yapici, Maillard, Anne M., Nowakowska, Beata, van den Bree, Marianne B.M., Swillen, Ann

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Avaliação do conhecimento dos anestesiologistas sobre cuidados paliativos von Santos, Maria de Fátima Oliveira dos, Teles, Natália Oliva, Oliveira, Harison José de, Gomes, Nicole de Castro, Tavares, Joana Cariri Valkasser, Nóbrega, Edilza Câmara

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Congenital diaphragmatic hernia in a patient with tetrasomy 9p von Henriques-Coelho, Tiago, Oliva-Teles, Natália, Fonseca-Silva, M. Luz, Tibboel, Dick, Guimarães, Hercília, Correia-Pinto, Jorge

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A Novel Frameshift CHD4 Variant Leading to Sifrim-Hitz-Weiss Syndrome in a Proband with a Subclinical Familial t(17;19) and a Large dup(2)(q14.3q21.1) von Da Silva, Jorge Diogo, Oliva-Teles, Natália, Tkachenko, Nataliya, Fino, Joana, Marques, Mariana, tuna, Ana Maria, David, Dezso

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Ambiguous Genitalia: An Unexpected Diagnosis in a Newborn von Losa, Ana, Da Silva Cardoso, Juliana, Leite, Sara, Barros, Ana Cristina, Guedes, Ana, Rodrigues, Cidade, Borges, Teresa, Oliva-Teles, Natália, Soares, Ana Rita, Mota, Céu

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Blueberry Muffin Syndrome and Hyperleukocytosis in a Newborn: A Diagnostic Challenge von Teixeira, Beatriz, Losa, Ana, Meireles, Andreia, Lachado, Ana, Couto Guerra, Isabel, Machado, Susana, Branco, Lídia, Paulino, Paulo, Lau, Catarina, Oliva-Teles, Natália, Mendes, Carlos, Oliva, Tereza, Pinho, Liliana, Neiva, Luísa, Proença, Elisa

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