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- 等位常染色體基因Hp1allelic autosomal genes; Hp1
- 等位常染色體基因Hp2Hp2
- 常用in common usage
- 常often
- 遺傳連鎖分析法對一常染色體顯性遺傳性視網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
- 雜合的在一個或更多的相應的染色體基因座上有不同的等位基因的Having different alleles at one or more corresponding chromosomal loci.
- 伴皮質下梗死和白質腦病的常染色體顯性遺傳性腦動脈病血液動力學研究The cerebral hemodynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- 染色體基因chromogene
- 同染色體基因syntenic genes
- 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
- Y染色體基因座Y-chromosome locus
- 常染色體STReuchromosome STR
- 正染色體基因autosomal gene amorphic
- 本病作為常染色體顯性傳遞。This disorder is inherited as an autosomal dominant trait.
- 伴X染色體基因X-linked genes
- 常染色體SNPsAutosomal SNPs
- 染色體基因擴增Gains of chromosome
- 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
- 染色體基因缺失Losses of chromosome
- 生物節律在常染色體顯性遺傳夜間額葉癲癎擇時用藥的意義Significance of Biological Rhythm on Selective Nocte Treatment on Autosomal Dominant Nocturnal Frontal Lobe Epilepsy