Your browser doesn't support javascript.
loading
Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiency.
Toledano, Helen; Orenstein, Naama; Sofrin, Efrat; Ruhrman-Shahar, Noa; Amarilyo, Gil; Basel-Salmon, Lina; Shuldiner, Alan R; Smirin-Yosef, Pola; Aronson, Melyssa; Al-Tarrah, Hibs; Bazak, Lili; Gonzaga-Jauregui, Claudia; Tabori, Uri; Wimmer, Katharina; Goldberg, Yael.
Afiliação
  • Toledano H; Department of Pediatric Hematology Oncology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Orenstein N; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Sofrin E; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Ruhrman-Shahar N; Pediatric Genetic Clinic, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Amarilyo G; Pediatric Genetic Clinic, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Basel-Salmon L; Recanati Genetics Institute, Rabin Medical Center, Petah Tikva, Israel.
  • Shuldiner AR; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Smirin-Yosef P; Felsenstein Medical Research Center, Rabin Medical Center, Petah Tikva, Israel.
  • Aronson M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Al-Tarrah H; Recanati Genetics Institute, Rabin Medical Center, Petah Tikva, Israel.
  • Bazak L; Regeneron Genetics Center, Tarrytown, New York, USA.
  • Gonzaga-Jauregui C; Department of Molecular Biology, Genomic Bioinformatics Laboratory, Ariel University, Ariel, Israel.
  • Tabori U; Zane Cohen Centre, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Wimmer K; Department of Haematology-Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Goldberg Y; Zane Cohen Centre, Mount Sinai Hospital, Toronto, Ontario, Canada.
J Med Genet ; 57(7): 505-508, 2020 07.
Article em En | MEDLINE | ID: mdl-31501241

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Neoplasias Encefálicas / Neoplasias Colorretais / Neurofibromatose 1 / Proteínas de Ligação a DNA / Lúpus Eritematoso Sistêmico Limite: Child / Child, preschool / Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Neoplasias Encefálicas / Neoplasias Colorretais / Neurofibromatose 1 / Proteínas de Ligação a DNA / Lúpus Eritematoso Sistêmico Limite: Child / Child, preschool / Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article