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Chromosome 7, monosomy

Known as: Monosomy 7 
A chromosomal abnormality consisting of the absence of one of the copies of chromosome 7 in somatic cells.
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Among 4,780 consecutive adult acute lymphoblastic/myeloblastic leukemia patients, we identified 117 (2.4%) patients with mixed… 
Highly Cited
2008
Highly Cited
2008
PURPOSE The transcription factor CCAAT/enhancer binding protein-alpha (CEBPA) is crucial for normal myeloid differentiation… 
Review
2007
Review
2007
Familial occurrence of myelodysplasia (MDS) and/or acute myeloid leukaemia (AML) is rare but can provide a useful resource for… 
Highly Cited
2005
Highly Cited
2005
sion. An abnormal karyotype developed in eight of our patients, usually preceding, and in every case associated with, leukemic… 
Highly Cited
2003
Highly Cited
2003
Primary myelodysplasia (MDS) without an increased number of blasts is a rare finding in childhood. We performed a retrospective… 
Highly Cited
2002
Highly Cited
2002
To ascertain the frequency of treatment-related acute myeloid leukemias and myelodysplastic syndromes (t-AML/t-MDS) in an… 
Review
1999
Review
1999
We reviewed the clinical features, treatment, and outcome of 100 children with myelodysplastic syndrome (MDS), juvenile… 
Highly Cited
1981
Highly Cited
1981
Summary. Between 1976 and 1979 a myeloproliferative disease associated with cells monosomic for chromosome number 7 in the bone…