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- 一例脆性X染色体综合征报告A CASE REPORT OF FRAGILE X SYNDROME
- 肺特异性X蛋白ltmg-specific X protein
- 多X染色体综合征poly X-chromosomal syndrome
- 三X染色体综合征triple X syndrome
- 骨髓水肿组与无骨髓水肿组的骨质破坏、跖趾关节(MTP)压痛、抗核周因子(APF)差异有显著性x~2值、P值分别为8.35、0.004:10.38、0.001;There were significant difference in the pain of metatarsal phalange joint, and APF between patients with MR1 bone marrow edema of wrists and patients without MR1 bone marrow edema of wrists ( x 2=10.38 p=0.001; x2=5.06 p=0.024) .
- 脆裂X染色体综合征fragile X syndrome
- Duchenne型肌营养不良症(DMD),是一种严重致死性X连锁隐性遗传病,发病率约为1/3500活男婴,其临床表现以肌肉的进行性萎缩和无力为特征。Duchenne muscular dystrophy is a common motal X - Linked recessive disease, whose incidence of male birth is 1/3500. It characterized by progressivelymuscular atrophy and weakness.
- 标志X染色体综合征Marker X syndrome
- 知性intellectuality
- 改性modification
- 染色体chromosome
- 脆性X染色体综合征fragile X syndrome
- E三染色体综合征,17-18三染色体综合征,18三染色体综合征E trisomy syndrome
- 脱离X染色体detached X
- X染色体X chromosome
- 脆X染色体fragile X chromosome
- 染色体综合征chromosome syndrome
- 复X染色体compound X-chromosomes
- 双X染色体double X
- D三染色体综合征D trisomy syndrome