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Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion.
Montenegro, Marília Moreira; Camilotti, Débora; Quaio, Caio Robledo D'Anglioli Costa; Gasparini, Yanca; Zanardo, Évelin Aline; Rangel-Santos, Andreia; Novo-Filho, Gil Monteiro; Francisco, Gleyson; Liro, Lucas; Nascimento, Amom; Chehimi, Samar Nasser; Soares, Diogo Cordeiro Queiroz; Krepischi, Ana C V; Grassi, Marcília Sierro; Honjo, Rachel Sayuri; Palmeira, Patricia; Kim, Chong Ae; Carneiro-Sampaio, Magda Maria Sales; Rosenberg, Carla; Kulikowski, Leslie Domenici.
Afiliação
  • Montenegro MM; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil; Laboratory of Medical Research in Pediatrics (LIM-36), Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil; Department of Pediatrics,
  • Camilotti D; Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo (USP), Sao Paulo - SP, Brazil.
  • Quaio CRDC; Albert Einstein Israeli Hospital, Sao Paulo, Brazil.
  • Gasparini Y; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Zanardo ÉA; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Rangel-Santos A; Laboratory of Medical Research in Pediatrics (LIM-36), Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Novo-Filho GM; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Francisco G; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Liro L; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Nascimento A; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Chehimi SN; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Soares DCQ; Department of Pediatrics, Children's Institute, Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Krepischi ACV; Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo (USP), Sao Paulo - SP, Brazil.
  • Grassi MS; Department of Pediatrics, Children's Institute, Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Honjo RS; Genetics Unit, Department of Pediatrics, Children's Institute, Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Palmeira P; Laboratory of Medical Research in Pediatrics (LIM-36), Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Kim CA; Genetics Unit, Department of Pediatrics, Children's Institute, Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Carneiro-Sampaio MMS; Department of Pediatrics, Children's Institute, Clinical Hospital of Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
  • Rosenberg C; Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo (USP), Sao Paulo - SP, Brazil.
  • Kulikowski LD; Cytogenomics Laboratory, Department of Pathology, Medicine School, University of Sao Paulo (FMUSP), Sao Paulo - SP, Brazil.
J Pediatr ; 252: 56-60.e2, 2023 01.
Article em En | MEDLINE | ID: mdl-36067875
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Cardiopatias Congênitas Tipo de estudo: Screening_studies Limite: Humans Idioma: En Revista: J Pediatr Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Cardiopatias Congênitas Tipo de estudo: Screening_studies Limite: Humans Idioma: En Revista: J Pediatr Ano de publicação: 2023 Tipo de documento: Article