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- 等位常染色体基因Hp1allelic autosomal genes; Hp1
- 等位常染色体基因Hp2Hp2
- 常用in common usage
- 常often
- 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
- 杂合的在一个或更多的相应的染色体基因座上有不同的等位基因的Having different alleles at one or more corresponding chromosomal loci.
- 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
- 染色体基因chromogene
- 同染色体基因syntenic genes
- 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
- Y染色体基因座Y-chromosome locus
- 常染色体STReuchromosome STR
- 正染色体基因autosomal gene amorphic
- 本病作为常染色体显性传递。This disorder is inherited as an autosomal dominant trait.
- 伴X染色体基因X-linked genes
- 常染色体SNPsAutosomal SNPs
- 染色体基因扩增Gains of chromosome
- 一种常染色体显性疾病an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system
- 染色体基因缺失Losses of chromosome
- 生物节律在常染色体显性遗传夜间额叶癫癎择时用药的意义Significance of Biological Rhythm on Selective Nocte Treatment on Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
