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- XP21/常染色体易位XP21/autosome translocation
- 常用in common usage
- 呈杂合子状态的某些常染色体易位完全可以生活的。Certain autosomal translocations in the heterozygous state can be fully viable.
- 常often
- 染色体chromosome
- 白血病染色体易位断裂点区域微卫星的不稳定性和杂合性丢失THE MICROSATELLITE INSTABILITY AND LOSS OF HETEROZYGOSITY IN CHROMOSOME TRANSLOCATION BREAKPOINT IN LEUKEMIA
- 常会regular session
- 辐射所致残存染色体易位与放射敏感性关系研究The Study on the Relationship of Residual Chromosome Aberration Induced by Irradiation with Radlosensltivity
- 伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病血液动力学研究The cerebral hemodynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- 遗传连锁分析法对一常染色体显性遗传性视网膜色素变性家系的基因定位研究Genetic linkage analysis of localizing an autosomal dominant retinitis pigmentosa gene in a family
- 9染色体易位9 translocation
- 常染色体autosome
- 组织培养创造抗白粉病小麦-簇毛麦染色体易位及分子标记辅助选择。Tissue culture induced translocation conferring powdery mildew resistance between wheat and dasypyrum villosum and its marker-assisted selection.
- SPARC在常染色体显性多囊肾病患者体液中的表达及其分泌研究Expression and secretion of SPARC in body fluid of patients with autosomal dominant polycystic kidney disease
- 急性早幼粒细胞白血病(APL)中t(15;17)染色体易位的分子机制研究Molecular Study of the Mechanism of Chromosomal Translocation (15; 17) in Acute Promyelocytic Leukemia (APL)
- 常染色体STReuchromosome STR
- 1BL/1RS染色体易位1BL/1RS chromosomal translocation
- 本病作为常染色体显性传递。This disorder is inherited as an autosomal dominant trait.
- 染色体易位i(17q-)Isochromosome 17q
- 常染色体SNPsAutosomal SNPs