Chromosome Studies on Acute Nonlymphocytic Leukaemia in Children
نویسندگان
چکیده
منابع مشابه
Chromosome studies in familial leukaemia.
The finding of an inherited chromosome abnormality (Chl) in several members of a family, including two who had developed chronic lymphocytic leukaemia (Gunz, Fitzgerald, and Adams, i962), led to the suggestion that this abnormality predisposed its carriers to the development of the disease, and that inherited cytogenetic abnormalities of this type might determine some instances of familial leuk...
متن کاملAcute myeloid leukaemia in children.
Acute myeloid leukaemia (AML) is characterized by a block in differentiation and an unregulated proliferation of myeloid progenitor cells. While the cause of AML in children is unknown, risk factors that have been identified include exposure to toxins such as ethanol, pesticides and dietary topoisomerase II inhibitors, prior chemotherapy with alkylating agents or topoisomerase II inhibitors, co...
متن کاملSex Chromosome Aneuploidy: Prospective Studies on Children
This two-volume publication contains the proceedings of a NATO Advanced Study Institute, held in April 1978. The material is organized in five sections. In the first section J. Bonner presents a historic review of chromatin research. The following section describes biophysical and chemical methods used in the study of isolated chromatin, such as electron microscopy, circular dichroism, X-ray di...
متن کاملPatients in Focus: What’s Relevant for Chronic Myeloid Leukaemia and Philadelphia Chromosome-positive Acute Lymphoblastic Leukaemia?
EMJ EUROPEAN MEDICAL JOURNAL HEMATOLOGY • August 2017 • Creative Commons Attribution-Non Commercial 4.0 EMJ EUROPEAN MEDICAL JOURNAL 52 53 PATIENTS IN FOCUS: WHAT’S RELEVANT FOR CHRONIC MYELOID LEUKAEMIA AND PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKAEMIA? This satellite symposium took place on 22nd June 2017 as part of the 22nd European Hematology Association (EHA) Congress in M...
متن کاملChromosome Aberrations and Prognostic Factors in Therapy-Related Myelodysplasia and Acute Nonlymphocytic Leukemia
Cytogenetic studies of 91 consecutive patients with therapy-related myelodysplasia or overt acute nonlymphocytic leukemia disclosed characteristic defects of chromosome 7 in 48 cases and of chromosome 5 in 21 cases. The chromosome 5 abnormalities were consistently present in all abnormal mitoses at the time of diagnosis, as were the chromosome 7 abnormalities in 45 of the 48 patients. Various a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Pediatric Research
سال: 1983
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-198305000-00016