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。
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。
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。
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。
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
染
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。
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突
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。
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。
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.
先性小眼球是一种先
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。
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。
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。