CYTOGENETICS OF <i>SCILLA SCILLOIDES</i> COMPLEX
نویسندگان
چکیده
منابع مشابه
Myelodyspastic syndrome with complex cytogenetics.
A 74-year-old man with colorectal carcinoma treated with surgery and adjuvant chemotherapy with oxaliplatin and fluorouracil 6 years previously was admitted with fever and suspicion of sepsis. Laboratory tests showed hemoglobin 137 g/L, mean corpuscular volume 94.7 fL, platelets 177 109/L, leukocytes 2.0 109/L, and neutrophils 0.8 109/L. Within 4 days his condition deteriorated rapidly with pro...
متن کاملAML cytogenetics: the complex just got simpler.
In this issue of Blood, Middeke et al, for the well-regarded Cooperative German Study Group, report a retrospective analysis in which they demonstrate that a hierarchial classification system for specific cytogenetic abnormalities in acute myeloid leukemia (AML) reveals that patients with abnormal 17p [abnl(17p)] and -5/5q- abnormalities have worse outcomes after allogeneic hematopoietic cell t...
متن کاملComplex cytogenetics in a patient with mixed-phenotype acute leukemia
which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 35-year-old woman had 2-month history of fever and bone pain, with an 8-kg weight loss in one month. Physical examination revealed 7-cm palpable spleen (splenomegaly). On admission, her hemoglobin level was 13.4 g/dL, white blood cell count was 144×10 9 /L...
متن کاملCytogenetics of multiple myeloma.
Great studies of multiple myeloma (MM) strongly suggested that specific chromosomal changes are of prognostic significance in patients with MM1. We have performed cytogenetic analysis and recently fluorescent in situ hybridization (FISH) on 43 cases of MM. Clonal chromosomal changes were present in 24 (56%) cases. Hyperdiploid karyotype was found in 12 (50%) cases, hypodiploid in 8 (33%) cases,...
متن کاملCytogenetics of hepatoblastoma.
The cytogenetics of hepatoblastoma demonstrate recurring events which include whole chromosome trisomies, most commonly trisomy of chromosome 2, 8, or 10. In addition, unbalanced translocations involving a breakpoint on the proximal short arm of chromosome 1 are observed which result in a duplication of the long arm of chromosome 1q. The most commonly involved reciprocal chromosomal arm is 4q, ...
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: The Japanese Journal of Genetics
سال: 1972
ISSN: 0021-504X,1880-5787
DOI: 10.1266/jjg.47.73