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Loss of Chromosome 7q

Known as: del(7q) 
A cytogenetic abnormality that refers to deletion of part of the long arm of chromosome 7. It is associated with the development of chronic… Expand
National Institutes of Health

Related topics

Related topics

11 relations
Chromosomes, Human, Pair 7Chronic Myelomonocytic Leukemia with EosinophiliaChronic Myelomonocytic Leukemia-1Chronic Myelomonocytic Leukemia-2
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Papers overview

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Highly Cited
2010
Highly Cited
2010
FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q).
Cytogenetic aberrations identified by metaphase cytogenetics (MC) have important diagnostic, prognostic and therapeutic roles in… Expand
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Highly Cited
2007
Highly Cited
2007
Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study.
Monosomy 7 (-7) and deletion 7q \del(7q)] are rare in childhood acute myeloid leukemia (AML). We retrospectively collected data… Expand
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Highly Cited
2002
Highly Cited
2002
Balanced chromosome abnormalities inv(16) and t(15;17) in therapy‐related myelodysplastic syndromes and acute leukemia: Report from an International Workshop †
The Workshop identified 48 unselected patients with therapy‐related myelodysplastic syndrome or acute myeloid leukemia (t‐MDS/t… Expand
Highly Cited
2002
Highly Cited
2002
Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q
We used spectral karyotyping (SKY) to study 29 adults with acute myeloid leukemia and a complex karyotype containing one to nine… Expand
Highly Cited
2001
Highly Cited
2001
Splenic marginal zone B-cell lymphomas: two cytogenetic subtypes, one with gain of 3q and the other with loss of 7q.
BACKGROUND AND OBJECTIVES Splenic marginal zone B-cell lymphoma (SMZBCL) has clinical, immunophenotypic and histologic features… Expand
Highly Cited
1999
Highly Cited
1999
Myelodysplastic and Myeloproliferative Disorders of Childhood: A Study of 167 Patients
Myelodysplastic syndromes (MDS) and myeloproliferative syndromes (MPS) of childhood are a heterogeneous group of clonal disorders… Expand
Highly Cited
1999
Highly Cited
1999
Myelodysplastic and myeloproliferative disorders of childhood: a study of 167 patients.
Myelodysplastic syndromes (MDS) and myeloproliferative syndromes (MPS) of childhood are a heterogeneous group of clonal disorders… Expand
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Review
1994
Review
1994
Secondary chromosomal abnormalities in acute leukemias.
Secondary chromosomal aberrations reported in the literature were surveyed in acute myeloid or lymphoblastic leukemia (AML or ALL… Expand
1994
1994
Translocations in 7q22 define a critical region in uterine leiomyomata.
Rearrangements involving the long arm of chromosome 7 in uterine leiomyoma are widely recognized and comprise one of the major… Expand
Highly Cited
1991
Highly Cited
1991
Chromosome 16 abnormalities associated with myeloid malignancies
Twenty‐six patients who had cytogenetic analyses performed for myeloid malignancies at St. Vincent's Hospital over a 6‐year… Expand
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