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Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.
Pastorczak, Agata; Hogendorf, Anna; Urbanska, Zuzanna; Budzynska, Edyta; Jesionek-Kupnicka, Dorota; Gach, Agnieszka; Hawula, Wanda; Smigiel, Robert; Skiba, Pawel; Sasiadek, Maria; Lejman, Monika; Constatinou, Maria; Lipska-Zietkiewicz, Beata S; Mlynarski, Wojciech.
Afiliação
  • Pastorczak A; Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.
  • Hogendorf A; Department of Pediatrics, Diabetology, Endocrinology and Nephrology, Medical University of Lodz, Lodz, Poland.
  • Urbanska Z; Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.
  • Budzynska E; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
  • Jesionek-Kupnicka D; Department of Pathology, Chair of Oncology, Medical University of Lodz, Lodz, Poland.
  • Gach A; Department of Medical Genetics, Polish Mother's Memorial Hospital-Research Institute, Lodz, Poland.
  • Hawula W; Department of Medical Genetics, Polish Mother's Memorial Hospital-Research Institute, Lodz, Poland.
  • Smigiel R; Department of Pediatrics, Division of Propaedeutic Pediatrics and Rare Disorders, Wroclaw Medical University, Wroclaw, Poland.
  • Skiba P; Department of Genetics, Wroclaw Medical University, Wroclaw, Poland.
  • Sasiadek M; Department of Genetics, Wroclaw Medical University, Wroclaw, Poland.
  • Lejman M; Laboratory of Genetic Diagnostics, Medical University of Lublin, Lublin, Poland.
  • Constatinou M; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
  • Lipska-Zietkiewicz BS; Centre for Rare Diseases, Medical University of Gdansk, Gdansk, Poland.
  • Mlynarski W; Clinial Genetics Unit, Department of Biology and Medical Genetics, Medical University of Gdansk, Gdansk, Poland.
Genes Chromosomes Cancer ; 60(2): 79-87, 2021 02.
Article em En | MEDLINE | ID: mdl-33135230
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Cromossomos Humanos Par 7 / Deficiências do Desenvolvimento / Deleção Cromossômica / Anormalidades Craniofaciais / Fator de Transcrição Ikaros / Leucemia-Linfoma Linfoblástico de Células Precursoras Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Cromossomos Humanos Par 7 / Deficiências do Desenvolvimento / Deleção Cromossômica / Anormalidades Craniofaciais / Fator de Transcrição Ikaros / Leucemia-Linfoma Linfoblástico de Células Precursoras Idioma: En Ano de publicação: 2021 Tipo de documento: Article