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adj.体的,体的
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome体;allele等位基因;chromosomal体的;mitochondrial线粒体的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 体显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体体显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于体显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异性眼科疾病,遗传方式有体显性遗传、体隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛发黑素沉着减少或缺乏引起的一类体隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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ferritiszation, ferritization, ferritize, ferritizer, ferritizing, ferrito-martensite, ferritremolite, ferritungstite, ferro, ferro-,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj.色体的,色体的
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome色体;allele等位基因;chromosomal色体的;mitochondrial线粒体的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 色体显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体色体显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于色体显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异性眼科疾病,遗传方式有色体显性遗传、色体隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类色体隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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ferroantigorite, ferroaugite, ferrobacillus, ferrobilin, ferroboral, ferroboron, ferrobrucite, ferrocal, ferrocalcite, ferrocarbo,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj. 正染色体的,常染色体的
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome染色体;allele等位基因;chromosomal染色体的;mitochondrial线粒体的;genetic的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 常染色体显性

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体染色体显性的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常染色体显性

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,方式有常染色体显性、常染色体隐性和X连锁隐性

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐形疾病的总称。

声明:以上句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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ferrochromium, ferrochrysotile, ferrocobalt, ferrocobaltite, ferrocoke, ferrocolumbite, ferrocolumbium, ferro-compound, ferroconcrete, ferrocrete,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj. 正染的,常染
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome;allele等位基因;chromosomal的;mitochondrial线粒的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 常染性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

牙本质形成不良是一种性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常染性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常染性遗传、常染隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛发黑素沉着减少或缺乏引起的一类常染隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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ferroelastic, ferroelasticity, ferroelastics, ferroelectric, ferroelectricity, ferro-electricity, ferroelectrics, ferroelectronic, ferroenamel, ferroferric,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj. 正染色体,常染色体
近义词
adj.
联想词
recessive后退;alleles对立形质;chromosome染色体;allele等位;chromosomal染色体;mitochondrial线粒体;genetic;mutation;genotype型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 常染色体显性遗

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体染色体显性遗胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常染色体显性遗

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗方式有常染色体显性遗、常染色体隐性遗和X连锁隐性遗

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关导致眼、皮肤、毛发黑色素沉着减少或缺乏引起一类常染色体隐形遗疾病总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件观点;若发现问题,欢迎向我们指正。

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ferrograph, ferro-graph, ferrography, ferro-graphy, ferrogum, ferrohastingsite, ferroheme, ferrohemoglobin, ferrohexahydrite, ferrohumite,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,

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ferro-silico-manganese, ferrosilicon, ferro-silicon-aluminium, ferro-silicon-nickel, ferro-silicon-titanium, ferro-silico-titanium, ferrosilite, ferrospinel, ferro-spinel, ferrostan,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,

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ferrugineus, ferruginol, ferruginosity, ferruginous, ferrule, ferrules, ferrum, ferrumiron, ferry, ferry boat,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj.的,常
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome;allele等位基因;chromosomal的;mitochondrial线粒的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧;ancestry祖先;
autosomal dominant inheritance 显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常显性遗传、常隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛发黑素沉着减少或缺乏引起的一类常隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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Fertile Crescent, fertileness, fertilisable, fertilisation, fertilise, fertiliser, fertility, fertility drug, fertility rate, fertility-rate,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj. 正染色体的,常染色体的
adj.
联想词
recessive后退的;alleles对立形质;chromosome染色体;allele等位基因;chromosomal染色体的;mitochondrial线粒体的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 常染色体显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常染色体显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

性小眼球是一种先异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合成相关基因突变导致眼、皮肤、毛黑色素沉着减少或缺乏引起的一类常染色体隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若现问题,欢迎向我们指正。

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fertilizer-responsive, fertilizin, fertonin, ferula, ferulaldehyde, ferule, ferulene, ferulenol, feruoyloxylupinane, ferutite,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj. 正染色体的,常染色体的
近义词
adj.
联想词
recessive后退的;alleles对立;chromosome染色体;allele等位基因;chromosomal染色体的;mitochondrial线粒体的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧核糖核酸;ancestry祖先;
autosomal dominant inheritance 常染色体显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本不良是一种体染色体显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常染色体显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑色素合相关基因突变导致眼、皮肤、毛发黑色素沉着减少或缺乏引起的一类常染色体隐遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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Fervidor, fervor, fervour, FES, fescennine, fescue, FESEM, fesogenin, fess, fesse,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,
adj.的,常
近义词
adj.
联想词
recessive后退的;alleles对立形质;chromosome;allele等位基因;chromosomal的;mitochondrial线粒的;genetic遗传的;mutation突变;genotype基因型;DNA脱氧酸;ancestry祖先;
autosomal dominant inheritance 显性遗传

Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.

摘要牙本质形成不良是一种显性遗传的中胚层缺陷。

Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.

手掌小鱼际区真实花纹可能属于常显性遗传。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常显性遗传、常隐性遗传和X连锁隐性遗传。

Oculocutaneous albinism(OCA) is a group of autosomal recessive disorders of melanin synthesis,which is characterized by congenital hypopigmentation of skin,hair and eyes.

眼皮肤白化病是由于黑素合成相关基因突变导致眼、皮肤、毛发黑素沉着减少或缺乏引起的一类常隐形遗传疾病的总称。

声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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festive, festivity, festivous, Festmeter, Festo, festology, festoon, festooner, festoonery, festschrift,

相似单词


autoslat, autosled, autosledge, autoslot, autosmia, autosomal, autosomatognosis, autosome, autosomnambulism, auto-sorter,