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Wilms tumor in patients with osteopathia striata with cranial sclerosis.
Bach, Alicia; Mi, Jingyi; Hunter, Matthew; Halliday, Benjamin J; García-Miñaúr, Sixto; Sperotto, Francesca; Trevisson, Eva; Markie, David; Morison, Ian M; Shinawi, Marwan; Willis, Daniel N; Robertson, Stephen P.
Afiliação
  • Bach A; Division of Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St Louis, MI, USA.
  • Mi J; Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, 9016, New Zealand.
  • Hunter M; Monash Genetics, Monash Medical Centre, Melbourne, VIC, Australia.
  • Halliday BJ; Department of Paediatrics, Monash University, Melbourne, VIC, Australia.
  • García-Miñaúr S; Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, 9016, New Zealand.
  • Sperotto F; Instituto de Genética Médica y Molecular, La Paz University Hospital, Madrid, Spain.
  • Trevisson E; Department of Women's and Children's Health, Padova University, Padova, Italy.
  • Markie D; Institute of Pediatric Research Città della Speranza, Clinical Genetics and Epidemiology Laboratory, Padova University, Padova, Italy.
  • Morison IM; Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Shinawi M; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, 9016, New Zealand.
  • Willis DN; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, 9016, New Zealand.
  • Robertson SP; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St Louis, MI, USA.
Eur J Hum Genet ; 29(3): 396-401, 2021 03.
Article em En | MEDLINE | ID: mdl-32879452
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteosclerose / Fenótipo / Tumor de Wilms Tipo de estudo: Etiology_studies / Guideline Limite: Adult / Child, preschool / Female / Humans / Infant Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido
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: Osteosclerose / Fenótipo / Tumor de Wilms Tipo de estudo: Etiology_studies / Guideline Limite: Adult / Child, preschool / Female / Humans / Infant Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido