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We report on the prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops… Expand We report on a midtrimester fetus with multiple malformations, who was prenatally found to have pure partial trisomy 1q with… Expand Partial trisomy of 1q is rare. Only 32 cases of isolated partial trisomy 1q have been previously reported. From these cases, a… Expand SummaryMinor abnormalities are described in an 11-month-old female in which a “de novo” trisomy 1q32→1qter and a monosomy 3p25… Expand During the last two decades, important progress has been made in the understanding of the nature and pathogenesis of idiopathic… Expand The prognostic significance of cytogenetic abnormalities was determined in 106 patients with well‐characterized idiopathic… Expand Idiopathic myelofibrosis is a chronic myeloproliferative disorder characterized by bone marrow fibrosis, extramedullary… Expand We report the use of fluorescent in situ hybridization (FISH) with a DNA library of chromosome 1-specific probes to confirm the… Expand Summary. Karyotypic analysis was performed in a total of 69 patients with well‐characterized idiopathic myelofibrosis. Karyotypic… Expand 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