Browsing by Author Cavalcanti, Denise P

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PreviewIssue DateTitleAuthor(s)AdvisorType
-1-Uns- -1Interphase-fish Study In Three Patients With Tetraploid/diploid Mosaicism.Cavalcanti, Denise P; Zanchetta, Luciene M-Artigo de periódico
2015Clinical And Molecular Characterization Of A Brazilian Cohort Of Campomelic Dysplasia Patients, And Identification Of Seven New Sox9 Mutations.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-Artigo de periódico
2015Six Additional Cases Of Sedc Due To The Same And Recurrent R989c Mutation In The Col2a1 Gene--the Clinical And Radiological Follow-up.Silveira, Karina C; Bonadia, Luciana C; Superti-Furga, Andrea; Bertola, Débora R; Jorge, Alexander A L; Cavalcanti, Denise P-Artigo de periódico
2013Non-immune Hydrops Fetalis: A Prospective Study Of 53 Cases.Moreno, Carolina A; Kanazawa, Thatiane; Barini, Ricardo; Nomura, Marcelo L; Andrade, Kléber C; Gomes, Cristiane P; Heinrich, Juliana K; Giugliani, Roberto; Burin, Maira; Cavalcanti, Denise P-Artigo de periódico
2012Clinical Epidemiology Of Skeletal Dysplasias In South America.Barbosa-Buck, Cecília O; Orioli, Iêda M; da Graça Dutra, Maria; Lopez-Camelo, Jorge; Castilla, Eduardo E; Cavalcanti, Denise P-Artigo de periódico
-1-Uns- -1[incidence Of Congenital Hydrocephalus And The Role Of The Prenatal Diagnosis].Cavalcanti, Denise P; Salomão, Maria A-Artigo de periódico
2011Mutation In Ift80 In A Fetus With The Phenotype Of Verma-naumoff Provides Molecular Evidence For Jeune-verma-naumoff Dysplasia Spectrum.Cavalcanti, Denise P; Huber, Celine; Sang, Kim-Hanh Le Quan; Baujat, Geneviève; Collins, Felicity; Delezoide, Anne-Lise; Dagoneau, Nathalie; Le Merrer, Martine; Martinovic, Jelena; Mello, Marcos Fernando S; Vekemans, Michel; Munnich, Arnold; Cormier-Daire, Valerie-Artigo de periódico
2007Early Exposure To Yellow Fever Vaccine During Pregnancy.Cavalcanti, Denise P; Salomão, Maria Antonieta; Lopez-Camelo, Jorge; Pessoto, Mônica A; ,-Artigo de periódico
2005Molecular Findings In Brazilian Patients With Osteogenesis Imperfecta.Reis, Fernanda C; Alexandrino, Fabiana; Steiner, Carlos E; Norato, Denise Y J; Cavalcanti, Denise P; Sartorato, Edi L-Artigo de periódico
Showing results 1 to 9 of 9