i(17q)

Known as: Isochromosome 17q 
A cytogenetic abnormality involving chromosome 17 that results from loss of the short arm and duplication of the long arm. This aberration is… (More)
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
AIM Our aim was to study prevalence, incidence, age at diagnosis, and mortality in Turner syndrome (TS) in Denmark. METHODS… (More)
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Highly Cited
2006
Highly Cited
2006
Medulloblastomas and supratentorial primitive neuroectodermal tumors are aggressive childhood tumors. We report our findings… (More)
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2005
2005
BACKGROUND Medulloblastomas are the most common primary malignant childhood intracranial neoplasms. Patients are currently sorted… (More)
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2005
2005
To better understand the genetic basis of medulloblastoma development, we sought genomic amplifications and deletions in these… (More)
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Highly Cited
2004
Highly Cited
2004
Although a great deal of information has accumulated regarding the mechanisms underlying constitutional DNA rearrangements… (More)
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Review
2002
Review
2002
Chronic myeloid leukemia (CML) is genetically characterized by the presence of the reciprocal translocation t(9;22)(q34;q11… (More)
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2001
2001
The incidence and role of p53 abnormalities have not been reported in splenic lymphoma with villous lymphocytes (SLVL), the… (More)
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Highly Cited
1996
Highly Cited
1996
Clinical and pathological features of 52 infants and children with atypical teratoid/rhabdoid tumor (ATT/RhT) of the central… (More)
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Highly Cited
1992
Highly Cited
1992
We present four cases of infantile cerebellar neoplasms composed of cells with large vesicular nuclei with prominent nucleoli… (More)
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1990
1990
Isochromosome 17q has previously been observed consistently in cytogenetic studies of medulloblastoma, the most common posterior… (More)
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