骨髓增生异常综合征患者因t(1;17)易位导致的1号染色体三体和17号染色体短臂单体联合存在。
Combined trisomy 1q and monosomy 17p due to translocation t(1;17) in a patient with myelodysplastic syndrome.
作者信息
Mamaev N, Mamaeva S E, Pavlova V A, Patterson D
机构信息
Cytogenetics Laboratory, 1st Pavlov Medical Institute, Leningrad, U.S.S.R.
出版信息
Cancer Genet Cytogenet. 1988 Oct 1;35(1):21-5. doi: 10.1016/0165-4608(88)90116-1.
PMID:3180004
Abstract
A nonconstitutional translocation, t(1;17)(q21;p11), has been observed in bone marrow cells from a young patient with myelodysplastic syndrome during a 4-year period. Cytogenetic findings and some clinical aspects are briefly discussed.
摘要
在一名患有骨髓增生异常综合征的年轻患者的骨髓细胞中，在4年的时间里观察到一种非染色体组型易位，即t(1;17)(q21;p11)。本文简要讨论了细胞遗传学发现和一些临床情况。
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