Evaluation of clinical checklists for fragile X syndrome screening in Brazilian intellectually disabled males: Proposal for a new screening tool von Christofolini, Denise M., Abbud, Eduardo M., Lipay, Monica V.N., Costa, Silvia S., Vianna-Morgante, Angela M., Bellucco, Fernanda T.S., Nogueira, Sintia I., Kulikowski, Leslie D., Brunoni, Décio, Juliano, Yára, Ramos, Marco A.P., Melaragno, Maria Isabel

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Pure duplication 1q41‐qter: Further delineation of trisomy 1q syndromes von Kulikowski, Leslie Domenici, Bellucco, Fernanda T.S., Nogueira, Sintia I., Christofolini, Denise M., Smith, Marilia de A.C., de Mello, Claudia B., Brunoni, Decio, Melaragno, Maria Isabel

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Deletion 22q11.2: Report of a complex meiotic mechanism of origin von Nogueira, Sintia Iole, Hacker, April M., Bellucco, Fernanda T. S., Kulikowski, Leslie Domenici, Christofolini, Denise Maria, Cernach, Mirlene C., Melaragno, Maria Isabel, Emanuel, Beverly S.

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Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum von Nogueira, Sintia Iole, Hacker, April M, Bellucco, Fernanda T.S, Christofolini, Denise M, Kulikowski, Leslie Domenici, Cernach, Mirlene C.S.P, Emanuel, Beverly S, Melaragno, Maria Isabel

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Atypical 22qll.2 deletion in a patient with DGS/VCFS spectrum von IOLE NOGUEIRA, Sintia, HACKER, April M, BELLUCCO, Fernanda T. S, CHRISTOFOLINI, Denise M, DOMENICI KULIKOWSKI, Leslie, CERNACH, Mirlene C. S. P, EMANUEL, Beverly S, MELARAGNO, Maria Isabel

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Clinical checklists in the selection of mentally retarded males for molecular screening of fragile X syndrome von Christofolini, Denise M., Lipay, Monica V.N., Ramos, Marco Antonio P., Costa, Silvia S., Bellucco, Fernanda T.S., Nogueira, Sintia I., Kulikowski, Leslie D., Brunoni, Décio, 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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Deletion 22q11.2: Report of a complex meiotic mechanism of origin von Nogueira, Sintia Iole, Hacker, April M., Bellucco, Fernanda T. S., Kulikowski, Leslie Domenici, Christofolini, Denise Maria, Cernach, Mirlene C., Melaragno, Maria Isabel, Emanuel, Beverly S.

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Mechanisms of structural chromosomal rearrangement formation von Burssed, Bruna, Zamariolli, Malú, Bellucco, Fernanda Teixeira, Melaragno, Maria Isabel

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Partial 5p Gain and 15q Loss in Three Patients from a Family with a t(5;15)(p13.3;q26.3) Translocation von Bellucco, Fernanda T., Favilla, Bianca P., Perrone, Eduardo, Melaragno, Maria I.

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Spread of X‐chromosome inactivation into autosomal regions in patients with unbalanced X‐autosome translocations and its phenotypic effects von Favilla, Bianca Pereira, Meloni, Vera Ayres, Perez, Ana Beatriz, Moretti‐Ferreira, Danilo, Souza, Deise Helena, Bellucco, Fernanda Teixeira, Melaragno, Maria Isabel

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Antibody indexes in COVID-19 convalescent plasma donors: Unanswered questions von Bonetti, Tatiana Carvalho de Souza, Latini, Flavia Roche Moreira, Invitti, Adriana Lukow, Fonseca, Marcelo Cunio Machado, Scorza, Fulvio Alexandre, Saldanha, Maira Garcia, Bellucco, Fernanda T., Bacarov, Natalia B.S., Soane, Michel M., Girão, Manoel João Batista Castelo

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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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Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature von Bellucco, Fernanda T., Mello, Claudia B., Meloni, Vera A., Melaragno, Maria Isabel

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Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype von Bellucco, Fernanda T., Rodrigues de Oliveira-Júnior, Hélio, Santos Guilherme, Roberta, Bragagnolo, Silvia, Alvarez Perez, Ana B., Ayres Meloni, Vera, Melaragno, Maria I.

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Fold-back mechanism originating inv-dup-del rearrangements in chromosomes 13 and 15 von Burssed, Bruna, Zamariolli, Malú, Favilla, Bianca Pereira, Meloni, Vera Ayres, Goloni-Bertollo, Eny Maria, Bellucco, Fernanda Teixeira, Melaragno, Maria Isabel

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Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature von Bellucco, Fernanda T., Fock, Rodrigo A., de Oliveira-Júnior, Hélio R., Perez, Ana B., Melaragno, Maria I.

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Copy number variation (CNV) identification, interpretation, and database from Brazilian patients von Godoy, Victória Cabral Silveira Monteiro de, Bellucco, Fernanda Teixeira, Colovati, Mileny, Oliveira-Junior, Hélio Rodrigues de, Moysés-Oliveira, Mariana, Melaragno, Maria Isabel

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Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome von Favilla, Bianca Pereira, Burssed, Bruna, Yamashiro Coelho, Érika Mitie, Perez, Ana Beatriz Alvarez, de Faria Soares, Maria de Fátima, Meloni, Vera Ayres, Bellucco, Fernanda Teixeira, Melaragno, Maria Isabel

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Serologic evidence of West Nile virus and Saint Louis encephalitis virus in horses from Southern Brazil von Weber, Matheus N., Mosena, Ana C. S., Baumbach, Letícia F., da Silva, Mariana S., Canova, Raíssa, dos Santos, Débora R. L., Budaszewski, Renata da F., de Oliveira, Livia V., Soane, Michel M., Saraiva, Natália B., Bellucco, Fernanda T., Mazurek, Bruno Amaral, Diehl, Gustavo N., Gil, Laura H. V. G., Borba, Mauro R., Corbellini, Luis G., Canal, Cláudio W.

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