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المؤلفون: Kurtz KJ; Department of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA., Tallis E; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Marcogliese AN; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA., Pulivarthi RH; Department of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA., Potocki L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Stevens AM; Department of Pediatrics, Section of Hematology/Oncology, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.

المصدر: Pediatric hematology and oncology [Pediatr Hematol Oncol] 2022 Nov; Vol. 39 (8), pp. 747-754. Date of Electronic Publication: 2022 Mar 11.

نوع المنشور: Case Reports; Letter

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 8700164 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-0669 (Electronic) Linking ISSN: 08880018 NLM ISO Abbreviation: Pediatr Hematol Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Burkitt Lymphoma* , Precursor Cell Lymphoblastic Leukemia-Lymphoma* , Rubinstein-Taybi Syndrome*/genetics , Rubinstein-Taybi Syndrome*/pathology, CREB-Binding Protein/genetics ; Child ; Chromosome Aberrations ; Female ; Genotype ; Haploidy ; Humans ; Mutation