Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics

Por Klein, Elisabeth, Manvelyan, Marina, Simonyan, Isabella, Hamid, Ahmed B, Guilherme, Roberta Santos, Liehr, Thomas, Karamysheva, Tatyana
Publicado em 2012

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

Terminal 18q deletions are stabilized by neotelomeres

Por Guilherme, Roberta Santos, Hermetz, Karen E, Varela, Patrícia Teixeira, Perez, Ana Beatriz Alvarez, Meloni, Vera Ayres, Rudd, M Katharine, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel
Publicado no Mol Cytogenet (2015)

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

Duplication 9p and their implication to phenotype

Por Guilherme, Roberta Santos, Meloni, Vera Ayres, Perez, Ana Beatriz Alvarez, Pilla, Ana Luiza, de Ramos, Marco Antonio Paula, Dantas, Anelisa Gollo, Takeno, Sylvia Satomi, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel
Publicado no BMC Med Genet (2014)

Cytogenomic Delineation and Clinical Follow-up of Two Siblings with an 8.5 Mb 6q24.2-q25.2 Deletion Inherited From a Paternal Insertion()

Por Meloni, Vera Ayres, Guilherme, Roberta Santos, Oliveira, Mariana Moyses, Migliavacca, Michele, Takeno, Sylvia Satomi, Sobreira, Nara Lygia Macena, Soares, Maria de Fatima Faria, de Mello, Claudia Berlim, Melaragno, Maria Isabel
Publicado no Am J Med Genet A (2014)

Complex small supernumerary marker chromosomes – an update

Por Liehr, Thomas, Cirkovic, Sanja, Lalic, Tanja, Guc-Scekic, Marija, de Almeida, Cynthia, Weimer, Jörg, Iourov, Ivan, Melaragno, Maria Isabel, Guilherme, Roberta S, Stefanou, Eunice-Georgia G, Aktas, Dilek, Kreskowski, Katharina, Klein, Elisabeth, Ziegler, Monika, Kosyakova, Nadezda, Volleth, Marianne, Hamid, Ahmed B
Publicado em 2013