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- 常染色體SNPsAutosomal SNPs
- 常用in common usage
- 常often
- 伴皮質(zhì)下梗死和白質(zhì)腦病的常染色體顯性遺傳性腦動(dòng)脈病血液動(dòng)力學(xué)研究The cerebral hemodynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- 遺傳連鎖分析法對一常染色體顯性遺傳性視網(wǎng)膜色素變性家系的基因定位研究Genetic linkage analysis of localizing an autosomal dominant retinitis pigmentosa gene in a family
- SPARC在常染色體顯性多囊腎病患者體液中的表達及其分泌研究Expression and secretion of SPARC in body fluid of patients with autosomal dominant polycystic kidney disease
- 常染色體STReuchromosome STR
- 本病作為常染色體顯性傳遞。This disorder is inherited as an autosomal dominant trait.
- 一種常染色體顯性疾病an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system
- 生物節律在常染色體顯性遺傳夜間額葉癲癎擇時(shí)用藥的意義Significance of Biological Rhythm on Selective Nocte Treatment on Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
- 一種常染色體退縮形式的肌營(yíng)養不良。an autosomal recessive form of muscular dystrophy characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle.
- XP21/常染色體易位XP21/autosome translocation
- 常染色體顯性多囊腎病Autosomal dominant polycystic kidney disease
- 角質(zhì)細胞生長(cháng)因子在常染色體顯性遺傳性多囊腎病囊腫組織中的表達定位Expression and localization of keratinocyte growth factor in renal cystic tissues of patients with autosomal dominant polycystic kidney disease
- 常染色體遺傳模型及穩定性Model and Stability of Autosome Heredity
- 一種常染色體顯性疾病。an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system.
- 常染色體顯性遺傳多囊腎病autosomal dominant polycystic kidney disease
- 常染色體隱性高膽固醇血癥autosomal recessive hypercholesterolemia
- 由于常染色體突變基因導致的疾病a disease caused by a dominant mutant gene on an autosome
- 由于常染色體突變基因導致的疾a disease caused by a dominant mutant gene on an autosome.
