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Partial Trisomy 1q

 
National Institutes of Health

Papers overview

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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
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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
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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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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
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Highly Cited
1997
Highly Cited
1997
The prognostic significance of cytogenetic abnormalities was determined in 106 patients with well-characterized idiopathic… Expand
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Review
1997
Review
1997
Idiopathic myelofibrosis is a chronic myeloproliferative disorder characterized by bone marrow fibrosis, extramedullary… Expand
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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
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1994
1994
Karyotypic analysis was performed in a total of 69 patients with well-characterized idiopathic myelofibrosis. Karyotypic… Expand
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1977
1977
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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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
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