Incidência de hidrocefalia congênita e o papel do diagnóstico pré-natal

by Cavalcanti,Denise P., Salomão,Maria A.
Published 2003

Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects

by Lucon,Danielle R., Zanchetta,Luciene M., Cavalcanti,Denise P.
Published 2006

Clinical and molecular characterization of a Brazilian cohort of campomelic dysplasia patients, and identification of seven new SOX9 mutations

by Mattos,Eduardo P., Sanseverino,Maria Teresa V., Magalhães,José Antônio A., Leite,Júlio César L., Félix,Temis Maria, Todeschini,Luiz Alberto, Cavalcanti,Denise P., Schüler-Faccini,Lavinia
Published 2015

A decade of molecular diagnosis of Mucolipidosis II and III in Brazil: a pooled analysis of 32 patients

by Ludwig,Nataniel F, Sperb-Ludwig,Fernanda, Randon,Dévora N, Bernardi,Pricila, Giuliani,Liane R, Moreno,Carolina A, Cavalcanti,Denise P, Silva,Luiz CS da, Schwartz,Ida V D
Published 2021

Identification of genomic imbalances in oral clefts

by Lustosa-Mendes,Elaine, Santos,Ana P. dos, Vieira,Társis P., Ribeiro,Erlane M., Rezende,Adriana A., Fett-Conte,Agnes C., Cavalcanti,Denise P., Félix,Têmis M., Monlleó,Isabella L., Gil-da-Silva-Lopes,Vera Lúcia
Published 2021