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- 阴性遗传[医] recessive inheritance
- 2例Ph染色体阴性的CGL患者 ,用RT PCR检测出bcr/abl融合基因。The bcr/abl fusion genes were found in patients with negative Philadelphia chromosome.
- 常用in common usage
- 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
- 常often
- 28例慢粒患者作细胞遗传学检查,26例Ph染色体阳性,2例Ph染色体阴性,阳性率为92.9%;Philadelphia chromosome was detected in 26 of 28 patients (92.9%25)by cytogenetic study.
- 遗传inheritance
- 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
- 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
- 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
- 常染色体STReuchromosome STR
- 本病作为常染色体显性传递。This disorder is inherited as an autosomal dominant trait.
- 常染色体SNPsAutosomal SNPs
- 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
- 一种常染色体退缩形式的肌营养不良。an autosomal recessive form of muscular dystrophy characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle.
- XP21/常染色体易位XP21/autosome translocation
- 常染色体显性多囊肾病Autosomal dominant polycystic kidney disease
- 角质细胞生长因子在常染色体显性遗传性多囊肾病囊肿组织中的表达定位Expression and localization of keratinocyte growth factor in renal cystic tissues of patients with autosomal dominant polycystic kidney disease
- 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.
- 常染色体遗传模型及稳定性Model and Stability of Autosome Heredity