Amanote Research
Register
Sign In
Translocation T(X;20)(q13;q13.3): A Nonrandom Abnormality in Four Patients With Myeloid Disorders: Case 1
Atlas of Genetics and Cytogenetics in Oncology and Haematology
- France
doi 10.4267/2042/38171
Full Text
Open PDF
Abstract
Available in
full text
Categories
Cancer Research
Oncology
Genetics
Hematology
Date
February 1, 2011
Authors
KS Reddy
KE Richkind
Publisher
INIST-CNRS
Related search
Translocation T(X;20)(q13;q13.3): A Nonrandom Abnormality in Four Patients With Myeloid Disorders: Case 3
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Translocation T(X;20)(q13;q13.3) as a Secondary Chromosome Abnormality in a Patient With 5q-: A Case Report
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
T(X;20)(q13;q13.3)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Mild Phenotypes Associated With an Unbalanced X-Autosome Translocation, 46,X,der(X)t(X;8)(q28;q13)
Clinical Case Reports
Medicine
T(X;11)(q13;q23)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
T(X;11)(q13;q23)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
Translocation T(11;14) (Q13;q32) and Genomic Imbalances in Multi-Ethnic Multiple Myeloma Patients: A Malaysian Study
Hematology Reports
Hematology
Small Cell Variant of Ki-1 Lymphoma Associated With Myelofibrosis and a Novel Constitutional Chromosomal Translocation T(3;4) (Q13;q12).
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
Three‑way Philadelphia Translocation T(9;10;22)(q34;p11.2;q11.2) as a Secondary Abnormality in an Imatinib Mesylate‑resistant Chronic Myeloid Leukemia Patient
Oncology Letters
Cancer Research
Oncology
