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Chromosome 9, trisomy

Known as: Chromosome 9 trisomy, Duplication 9, Trisomy 9 
A chromosomal abnormality consisting of the presence of a third copy of chromosome 9 in somatic cells.
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
OBJECTIVE To determine whether non-invasive prenatal testing by maternal plasma DNA sequencing can uncover all fetal chromosome… Expand
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Highly Cited
2006
Highly Cited
2006
The identification of an acquired mutation of JAK2 in patients with myeloproliferative disorders has raised questions about the… Expand
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2006
2006
Although cytogenetic analysis advanced the understanding of the pathogenesis of primary non-Hodgkin lymphoma and led to improved… Expand
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Highly Cited
2005
Highly Cited
2005
BACKGROUND AND OBJECTIVES The main prognostic factors in myelodysplastic syndromes (MDS) are chromosomal abnormalities, the… Expand
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Highly Cited
2005
Highly Cited
2005
Primary mediastinal B-cell lymphoma (PMBL) is a well-defined subtype of diffuse large B-cell lymphoma. Molecular cytogenetics… Expand
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1985
1985
A new patient with trisomy for the chromosome segment 9pter----q22 is compared to 19 previously reported cases of partial trisomy… Expand
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1983
1983
A term female infant with intrauterine growth retardation and multiple congenital anomalies had trisomy 9 mosaicism in blood and… Expand
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1976
1976
SummaryTwo infants with trisomy involving chromosome 9 are described. One had complete trisomy 9 and the other karyotype 47,XX… Expand
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1975
1975
A kindred with an X-autosome translocation and differential inactivation of the X chromosome is described. The phenotypically… Expand
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Highly Cited
1973
Highly Cited
1973
The first patient with trisomy 9, an infant who survived 28 days, is reported. Clinical findings included microcephaly, low-set… Expand
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