induced aberration诱发畸变 nduced mutaion诱发突变 ndustrial genomics工业基因组学 inherited disorders of collage胶原蛋白病 Insertion插入 interstitial deletion中间缺失 intrauterine diagnosis宫内诊断 inversion倒位 rregular dominance不规则显性 isochromosome等臂染色体 karyotype核型 karyotype analysis核型分析 Kearns-Sayre syndrome, Kss Kearns-Sayre综合征 Klinefelter syndrome Klinefelter综合征 Kpn I family Kpn I家族 landmark界标 Leber hereditary optic neuropathy, LHON Leber遗传性视神经病 Leigh syndrom, LS Leigh综合征 h- Nyhan syndrome Lesch- Nyhan综合征 liability易患性 length- based heteroplasmy长度异质性 linkage map连锁图 loss-of- function mutation功能丢失的突变 luxury protein奢侈蛋白 major gene主基因 major histocompatibility complex,MHC主要组织相容性复合体 maternal inheritance母系遗传 medical genetics医学遗传学 metacentric chromosome中着丝粒染色体 minor gene微效基因 missense mutation错义突变 mitochondrial disease线粒体病 mitochondrial dna, mtDNA线粒体DNA mitochondrial encephalomyopathies,ME线粒体脑肌病 mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes, MELAS s&Finduced aberration 诱发畸变 induced mutaion 诱发突变 industrial genomics 工业基因组学 inherited disorders of col1age 胶原蛋白病 insertion 插入 interstitial deletion 中间缺失 intrauterine diagnosis 宫内诊断 inversion 倒位 irregular dominance 不规则显性 isochromosome 等臂染色体 K karyotype 核型 karyotype analysis 核型分析 Kearns-Sayre syndrome，KSS Kearns-Sayre 综合征 Klinefelter syndrome Klinefelter 综合征 KpnⅠ family KpnⅠ家族 L landmark 界标 Leber hereditary optic neuropathy，LHON Leber 遗传性视神经病 Leigh sysdrom，LS Leigh 综合征 Lesch-Nyhan syndrome Lesch-Nyhan 综合征 liability 易患性 length-based heteroplasmy 长度异质性 linkage map 连锁图 loss-of-function mutation 功能丢失的突变 luxury protein 奢侈蛋白 M major gene 主基因 major histocompatibility complex，MHC 主要组织相容性复合体 maternal inheritance 母系遗传 medical genetics 医学遗传学 metacentric chromosome 中着丝粒染色体 minor gene 微效基因 missense mutation 错义突变 mitochondrial disease 线粒体病 mitochondrial DNA，mtDNA 线粒体 DNA mitochondria1 encephalomyopathies，ME 线粒体脑肌病 mitochondrial encephalomyopathy with lactic acidosis，and stroke-like episodes，MELAS 线粒