Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report

Por Guilherme, Roberta S, Meloni, Vera de FA, Takeno, Sylvia S, Pellegrino, Renata, Brunoni, Decio, Kulikowski, Leslie D, Melaragno, Maria I
Publicado em 2012

A novel de novo mutation in MYT1, the unique OAVS gene identified so far

Por Berenguer, Marie, Tingaud-Sequeira, Angele, Colovati, Mileny, Melaragno, Maria I, Bragagnolo, Silvia, Perez, Ana B A, Arveiler, Benoit, Lacombe, Didier, Rooryck, Caroline
Publicado no Eur J Hum Genet (2017)

Mechanisms of ring chromosome formation, ring instability and clinical consequences

Por Guilherme, Roberta S, Ayres Meloni, Vera F, Kim, Chong A, Pellegrino, Renata, Takeno, Sylvia S, Spinner, Nancy B, Conlin, Laura K, Christofolini, Denise M, Kulikowski, Leslie D, Melaragno, Maria I
Publicado em 2011

Marfan syndrome with a complex chromosomal rearrangement including deletion of the <it>FBN1 </it>gene

Por Colovati Mileny ES, da Silva Luciana RJ, Takeno Sylvia S, Mancini Tatiane I, N Dutra Ana R, Guilherme Roberta S, de Mello Cláudia B, Melaragno Maria I, A Perez Ana B
Publicado em 2012-01-01

Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene

Por Colovati, Mileny ES, da Silva, Luciana RJ, Takeno, Sylvia S, Mancini, Tatiane I, N Dutra, Ana R, Guilherme, Roberta S, de Mello, Cláudia B, Melaragno, Maria I, A Perez, Ana B
Publicado em 2012

PRODH Polymorphisms, Cortical Volumes and Thickness in Schizophrenia

Por Ota, Vanessa K., Bellucco, Fernanda T., Gadelha, Ary, Santoro, Marcos L., Noto, Cristiano, Christofolini, Denise M., Assunção, Idaiane B., Yamada, Karen M., Ribeiro-dos-Santos, Ândrea K., Santos, Sidney, Mari, Jair J., Smith, Marília A. C., Melaragno, Maria I., Bressan, Rodrigo A., Sato, João R., Jackowski, Andrea P., Belangero, Sintia I.
Publicado em 2014