der(1)t(1;19)(p12;p11)：骨髓增生异常综合征中的一种新的非随机染色体异常。
der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in myelodysplastic syndrome.
作者信息
Gill J I, Varela M, Tsien F, Krause J R
机构信息
Department of Pathology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
出版信息
Cancer Genet Cytogenet. 1997 Apr;94(2):85-7. doi: 10.1016/s0165-4608(96)00188-4.
PMID:9109932
Abstract
The der(1)t(1;19)(p12;p11) has not been previously reported in myelodysplastic syndrome (MDS). Fluorescence in situ hybridization (FISH) using chromosome 1- and chromosome 19-specific probes, performed on the bone marrow (BM) cells of this patient confirmed the initial karyotype, i.e., 47,XY,+der(1)t(1;19)(p12;p11).
摘要
der(1)t(1;19)(p12;p11)此前未在骨髓增生异常综合征（MDS）中报道过。使用1号染色体和19号染色体特异性探针，对该患者的骨髓（BM）细胞进行荧光原位杂交（FISH），证实了初始核型，即47,XY,+der(1)t(1;19)(p12;p11)。
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