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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

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Broader (2)

Chromosomes, Human, Pair 9Trisomy

Papers overview

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Review
2007
Review
2007
Chromosomal abnormalities associated with neural tube defects (I): full aneuploidy.
Highly Cited
2005
Highly Cited
2005
Biallelic mutation of SOCS-1 impairs JAK2 degradation and sustains phospho-JAK2 action in the MedB-1 mediastinal lymphoma line.
Primary mediastinal B-cell lymphoma (PMBL) is a well-defined subtype of diffuse large B-cell lymphoma. Molecular cytogenetics… 
Highly Cited
2004
Highly Cited
2004
[Biallelic mutation of SOCS-1 impairs JAK2 degradation and sustains phospho-JAK2 action in MedB-1 mediastinal lymphoma line].
Primary mediastinal B-cell lymphoma (PMBL) is a well-defined subtype of diffuse large B-cell lymphoma. Molecular cytogenetics… 
Highly Cited
2003
Highly Cited
2003
Absence of fetal nasal bone and aneuploidies at first‐trimester nuchal translucency screening in unselected pregnancies
The absence of nasal bone (NB) has been noted in trisomy 21 fetuses at first‐trimester ultrasound, in high‐risk pregnancies. In… 
Review
1995
Review
1995
Trisomy 9: review and report of two new cases.
Trisomy 9 is a relatively uncommon chromosome abnormality that may sometimes be seen in the nonmosaic state. We reviewed 23… 
Highly Cited
1985
Highly Cited
1985
The phenotypic and cytogenetic spectrum of partial trisomy 9.
A new patient with trisomy for the chromosome segment 9pter----q22 is compared to 19 previously reported cases of partial trisomy… 
Highly Cited
1983
Highly Cited
1983
Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome.
A term female infant with intrauterine growth retardation and multiple congenital anomalies had trisomy 9 mosaicism in blood and… 
Review
1977
Review
1977
Trisomy 9 syndrome
An infant is described with multiple congenital anomalies associated with mosaic trisomy 9. Review of the three previously… 
Highly Cited
1975
Highly Cited
1975
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
A kindred with an X-autosome translocation and differential inactivation of the X chromosome is described. The phenotypically… 
Highly Cited
1973
Highly Cited
1973
A Case of Trisomy 9
The first patient with trisomy 9, an infant who survived 28 days, is reported. Clinical findings included microcephaly, low-set… 
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