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trisomy 11

The presence of a third copy of chromosome 11 in somatic cells.
National Institutes of Health

Related topics

Related topics

3 relations
Cellular Congenital Mesoblastic NephromaChromosomes, Human, Pair 11infantile fibrosarcoma

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Acute myeloid leukemia arising from a donor derived premalignant hematopoietic clone: A possible mechanism for the origin of leukemia in donor cells
Highly Cited
2007
Highly Cited
2007
Upregulation of translational machinery and distinct genetic subgroups characterise hyperdiploidy in multiple myeloma
Karyotypic instability, including numerical and structural chromosomal aberrations, represents a distinct feature of multiple… 
2005
2005
High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.
1999
1999
Isochromosome 8q formation is associated with 8p loss of heterozygosity in a prostate cancer cell line
In advanced prostate cancer, loss of chromosomal regions on 8p is frequently associated with gain of 8q. We studied the gross… 
1995
1995
Cytogenetic findings in a case of congenital mesoblastic nephroma.
1995
1995
Nonrandom chromosomal change (trisomy 11) in murine plasmacytomas induced by an ABL-MYC retrovirus.
Trisomy of chromosome 11 (Ts11) is the second most frequent nonrandom chromosomal change in murine plasmacytomas (PCTs). The… 
Review
1992
Review
1992
Cytogenetic biclonality in malignant hematologic disorders.
1990
1990
Karyotypically unrelated clones in acute leukemias and myelodysplastic syndromes.
1985
1985
Double nondisjunction during karyotypic progression of chemically induced Syrian hamster cell lines.
1974
1974
Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13
SummaryA complex structural rearrangement of chromosomes 11, 12 and 13 was found in a normal female who gave birth to an affected… 
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