Search


Current filters:

Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 1-10 of 39 (Search time: 0.004 seconds).
Issue DateTitleAuthor(s)
2013Clinical, cytogenetic and molecular characterization of three patients with r(22), including one with 22q11.2 deletionGUILHERME, Roberta Santos; KIM, Chong Ae; BRUNONI, Decio; SPINNER, Nancy Bettina; CONLIN, Laura Kathleen; DABER, Robert; CHRISTOFOLINI, Denise Maria; KULIKOWSKI, Leslie Domenici; MELARAGNO, Maria Isabel
2018BLM, FOXO3, FOXK2, FOXM1, FOXR1 genes as therapeutic targets to neuroblastomaGIMENEZ, Thamiris Magalhaes; NEVES, Nathalia Halley; SANTOS, Andreia Rangel; MARCHI, Fabio A.; KULIKOWSKI, Leslie; CRISTOFANI, Lilian M.; NOVAK, Estela M.; ODONE FILHO, Vicente
2013The role of CNVs in molecular mechanisms for rearrangements in 22q11.2 region diseasesDUTRA, Roberta; ZANARDO, Evelin; PIAZZON, Flavia; DIAS, Alexandre; MONTENEGRO, Marilia; NOVO-FILHO, Gil; BASSO, Mariana; COSTA, Thais; NASCIMENTO, Amon; KIM, Chong; KULIKOWSKI, Leslie; MELARAGNO, Maria Isabel; MELO, Joana Barbosa
2013Cytogenomic Diagnosis of Congenital Heart DiseasesKULIKOWSKI, Leslie; ZANARDO, Evelin; DUTRA, Roberta; PIAZZON, Flavia; DIAS, Alexandre; MONTENEGRO, Marilia; NOVO-FILHO, Gil; BASSO, Mariana; COSTA, Thais; NASCIMENTO, Amom; GRASSI, Marcilia; CARNEIRO-SAMPAIO, Magda; KIM, Chong
2017Lymphoproliferative Disorder with Hypogammaglobulinemia: an Unusual Presentation of 22q11.2 Deletion SyndromeSOARES, Diogo C.; NUNEZ, Evelyn Cristina; SANTOS, Cristiane J.; PASTORINO, Antonio C.; DANTAS, Anelisa G.; TORRES, Leuridan C.; ZANARDO, Evelin A.; KULIKOWSKI, Leslie D.; MELARAGNO, Maria Isabel; CARNEIRO-SAMPAIO, Magda M. S.; KIM, Chong Ae
201716q24 DUPLICATION AND IVEMARK SYNDROME: A NOVEL GENOMIC CAUSE?SOARES, Diogo C.; PIAZZON, Flavia B.; ZANARDO, Evelin; PASTORINO, Antonio Carlos; KULIKOWSKI, Leslie D.; BERTOLA, Debora R.; CARNEIRO-SAMPAIO, Magda; KIM, Chong Ae
2015HERPES ZOSTER INFECTION IN CHILDHOOD AND ADULT SYSTEMIC LUPUS ERYTHEMATOSUS: HIGHER PREVALENCE AND DISTINCT FEATURESGORMEZANO, N. W.; SILVA, C. A.; OTSUZI, C. I.; BARROS, D. L.; SILVA, M. A. Da; SALLUM, A. M.; PASOTO, S.; PEREIRA, R. M.; BONFA, E.
2015ACTIVE SEARCH FOR 22q11.2 DELETION IN INFANTS WITH CONGENITAL HEART DISEASE UNDERGOING CORRECTIVE SURGERY: PRELIMINARY RESULTSGRASSI, Marcilia Sierro; KULIKOWSKI, Leslie Domenici; JACOB, Cristina Miuki Abe; DUTRA, Roberta Lelis; ZANARDO, Evelin; CECCON, Maria Esther Jurfest Rivero; KREBS, Vera Lucia Jornada; IKARI, Nana Miura; JATENE, Marcelo Biscegli; CARVALHO, Werther Brunow; CARNEIRO-SAMPAIO, Magda
2013Detection of 22q11.2 Deletion in Infants with Congenital Heart Disease (Preliminary Data)CARNEIRO-SAMPAIO, M.; GRASSI, M. Sierro; KULIKOWSKI, L. Domenici; JACOB, C. Miuki Abe; DUTRA, R. Lelis; MIURA, N.; CECCON, M. E. Jurfest Rivero; KREBS, V. L. Jornada; CARVALHO, W. Brunow; JATENE, M.
2019Phenotype Assessment of a Brazilian Cornelia de Lange Syndrome (CDLS) cohortKIM, V. E. H.; FURQUIM, I.; CERONI, J. R. M.; CASTRO, P. H. S.; OLIVATI, C.; BERLIM, C.; LOPES, D. M. B.; PIMENTA, L.; HONJO, R. S.; BERTOLA, D. R.; KIM, C. A.