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Cornelia de Lange syndrome and cancer: An open question.
Pallotta, Maria M; Di Nardo, Maddalena; Hennekam, Raoul C M; Kaiser, Frank J; Parenti, Ilaria; Pié, Juan; Ramos, Feliciano J; Kline, Antonie D; Musio, Antonio.
Afiliação
  • Pallotta MM; Institute for Biomedical Technologies, National Research Council, Pisa, Italy.
  • Di Nardo M; Institute for Biomedical Technologies, National Research Council, Pisa, Italy.
  • Hennekam RCM; Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Kaiser FJ; Institute for Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Parenti I; Essen Center for Rare Diseases (Essener Zentrum für Seltene Erkrankungen, EZSE), University Hospital Essen, Essen, Germany.
  • Pié J; Institute for Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Ramos FJ; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, University of Zaragoza, CIBERER-GCV02 and ISS-Aragon, Zaragoza, Spain.
  • Kline AD; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, University of Zaragoza, CIBERER-GCV02 and ISS-Aragon, Zaragoza, Spain.
  • Musio A; Clinical Genetics Unit, Service of Paediatrics, University Hospital "Lozano Blesa", University of Zaragoza, CIBERER GCV02 and ISS-Aragón, Zaragoza, Spain.
Am J Med Genet A ; 191(1): 292-295, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36253936
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Cornélia de Lange / Neoplasias Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Cornélia de Lange / Neoplasias Idioma: En Ano de publicação: 2023 Tipo de documento: Article