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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
2016
Highly Cited
2016
Germline GATA2 mutations cause cellular deficiencies with high propensity for myeloid disease. We investigated 426 children and… Expand
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Highly Cited
2010
Highly Cited
2010
Gene-modified autologous hematopoietic stem cells (HSC) can provide ample clinical benefits to subjects suffering from X-linked… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
1997
Highly Cited
1997
The improved outcome of acquired aplastic anemia (AA) has revealed later complications, such as myelodysplastic syndrome (MDS… Expand
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Review
1997
Review
1997
Chronic myelomonocytic leukemia (CMML) is a rare hematopoietic malignancy of childhood. To define the clinical and hematologic… Expand
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Review
1997
Review
1997
ABOUT 40 YEARS ago two forms of chronic myelocytic leukemia (CML) were recognized in children. One had the typical features of… Expand
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Highly Cited
1996
Highly Cited
1996
We performed a randomized study of hydroxyurea (HY) versus VP16 in advanced chronic myelomonocytic leukemia (CMML) patients with… Expand
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