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Partial Trisomy 1q

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
We report on the prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops… Expand
Review
2005
Review
2005
We report on a midtrimester fetus with multiple malformations, who was prenatally found to have pure partial trisomy 1q with… Expand
Review
2005
Review
2005
Partial trisomy of 1q is rare. Only 32 cases of isolated partial trisomy 1q have been previously reported. From these cases, a… Expand
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2004
2004
SummaryMinor abnormalities are described in an 11-month-old female in which a “de novo” trisomy 1q32→1qter and a monosomy 3p25… Expand
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Review
1998
Review
1998
During the last two decades, important progress has been made in the understanding of the nature and pathogenesis of idiopathic… Expand
Highly Cited
1997
Highly Cited
1997
The prognostic significance of cytogenetic abnormalities was determined in 106 patients with well‐characterized idiopathic… Expand
Review
1997
Review
1997
  • J. Reilly
  • Blood reviews
  • 1997
  • Corpus ID: 13730167
Idiopathic myelofibrosis is a chronic myeloproliferative disorder characterized by bone marrow fibrosis, extramedullary… Expand
Review
1994
Review
1994
We report the use of fluorescent in situ hybridization (FISH) with a DNA library of chromosome 1-specific probes to confirm the… Expand
1994
1994
Summary. Karyotypic analysis was performed in a total of 69 patients with well‐characterized idiopathic myelofibrosis. Karyotypic… Expand
1977
1977
Minor abnormalities are described in an 11-month-old female in which a "de novo" trisomy 1q32 leads to lqter and a monosomy 3p25… Expand