换一批
换一批Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14.
第一作者：
E J,Sinclair
第一单位：
North Trent Cytogenetics Service, and Department of Haematology, Royal Hallamshire Hospital, Sheffield, UK.
作者：
主题词
成年人(Adult);老年人(Aged);老年人, 80以上(Aged, 80 and over);染色体畸变(Chromosome Aberrations);染色体障碍(Chromosome Disorders);染色体, 人, 13对(Chromosomes, Human, Pair 13);女(雌)性(Female);基因缺失(Gene Deletion);人类(Humans);原位杂交, 荧光(In Situ Hybridization, Fluorescence);男(雄)性(Male);中年人(Middle Aged);原发性骨髓纤维化(Primary Myelofibrosis);易位, 遗传(Translocation, Genetic)
DOI
10.1046/j.1365-2141.2001.02754.x
PMID
11380400
发布时间
2019-07-05
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