Trisomy
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Subject Areas on Research
- A de novo direct duplication of 16q22.1 --> q23.1 in a boy with midface hypoplasia and mental retardation.
- Abnormal amniotic fetal antigen 2 concentrations in trisomy 18 and trisomy 21.
- Abnormal production of interleukin-1 by microglia from trisomy 16 mice.
- Composite lymphoma of follicular B-cell and peripheral T-cell types with distinct zone distribution in a 75-year-old male patient: a case study.
- Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.
- Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
- Cytogenetics and mechanisms of spontaneous abortions: increased apoptosis and decreased cell proliferation in chromosomally abnormal villi.
- Detection of trisomy 12 by fluorescence in situ hybridization on archival cytopathologic material in chronic lymphocytic leukemia/small lymphocytic lymphoma.
- Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group.
- Enhanced production of superoxide anion by microglia from trisomy 16 mice.
- Evidence for a striking increase in acetylcholinesterase activity in cultured human fibroblasts which are trisomic for chromosome two.
- Fetal choroid plexus lesions. Relationship of antenatal sonographic appearance to clinical outcome.
- Increased expression of NR2A subunit does not alter NMDA-evoked responses in cultured fetal trisomy 16 mouse hippocampal neurons.
- Interphase fluorescence in situ hybridization for trisomy 12 on archival ovarian sex cord-stromal tumors.
- Isolated trisomy of chromosomes 8, 11, 13 and 21 is an adverse prognostic factor in adults with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B 8461.
- Malignant giant cell tumor of synovium (malignant pigmented villonodular synovitis).
- Management Considerations for Ongoing Pregnancies Complicated by Trisomy 13 and 18.
- Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18.
- Mosaic trisomy 9 hematopoietic chimera.
- Prenatal diagnosis of complete sole trisomy 1q.
- Prenatal diagnosis of mosaic trisomy 13: a case report.
- Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461).
- Prolonged pancytopenia in a gene therapy patient with ADA-deficient SCID and trisomy 8 mosaicism: a case report.
- Redox regulation of neuronal migration in a Down Syndrome model.
- Simultaneous presence of major secondary chromosomal abnormalities in blast crisis of chronic myeloid leukemia.
- Transfusion medicine illustrated: Mosaic Trisomy 9 in an infant with mixed-field ABO blood grouping.
- Trisomy 15 associated with nonimmune hydrops.
- Trisomy 8 mosaicism: selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells.
- Trisomy of rat chromosome 1 associated with mesothelial cell transformation.
- Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature review.