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Chromosome 8, trisomy

Known as: chromosome 8 trisomy syndrome, TRISOMY 8 SYNDROME, Chromosome 8 duplication 
A chromosomal abnormality consisting of the presence of a third copy of chromosome 8 in somatic cells.
National Institutes of Health

Related topics

Related topics

29 relations
Acute Myeloid Leukemia with Minimal DifferentiationBlast PhaseChest Wall FibromatosisDensely Granulated Pituitary Gland Lactotroph Adenoma

Broader (2)

Chromosomes, Human, Pair 8Trisomy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
Trisomy 8 in acute myeloid leukaemia.
Two cases of acute myeloid leukaemia with trisomy 8 in all examined bone marrow cells are reported. The occurrence and the… 
Highly Cited
2006
Highly Cited
2006
CD34 cells from patients with trisomy 8 myelodysplastic syndrome (MDS) express early apoptotic markers but avoid programmed cell death by up-regulation of antiapoptotic proteins.
CD34 cells from patients with trisomy 8 myelodysplastic syndrome (MDS) are distinguished from other MDS cells and from normal… 
2001
2001
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.
1997
1997
Clinicopathological and interphase cytogenetic analysis of desmoid tumours
Recurrence of desmoid tumours is difficult to predict from only histological findings. In this study, immunohistochemistry for… 
1995
1995
Acute leukemia and the transient myeloproliferative disorder associated with Down syndrome: morphologic, immunophenotypic and cytogenetic manifestations.
Individuals with Down syndrome have an increased incidence of leukemia compared to the general population. In addition, Down… 
Review
1994
Review
1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development.
Two patients with trisomy 8 syndrome owing to an isodicentric 8p;8p chromosome are described. Case 1 had a 46,XX/46,XX,-8,+idic(8… 
1994
1994
Myelodysplasia in a patient with pre‐existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease
SUMMARY. Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired haemolytic anaemia, clonal in nature, due to somatic mutation… 
1988
1988
Trisomy 8 Mosaicism Syndrome
The paper presents clinical manifestations and results of cytogenetic examination of two patients with trisomy 8 mosaicism… 
1987
1987
Molecular characteristics of chronic myelogenous leukemia in blast crisis.
1985
1985
Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism.
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