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遗传
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染色体显遗传
中胚层缺陷。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天球是一种先天发育异常
科疾病,遗传方式有常染色体显
遗传、常染色体隐
遗传和X连锁隐
遗传。
Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.
手掌鱼际区真实花纹可能属于常染色体显
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.
皮肤白化病是由于黑色素合成相关基因突变导致
、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传疾病
总称。
声明:以上例句、词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体染色体显性遗中
陷。
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
。
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。
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变导致眼、皮肤、毛发黑色素沉着减少或
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体染色体显性遗中
陷。
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
。
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。
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变导致眼、皮肤、毛发黑色素沉着减少或
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。
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。
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。
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。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天性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。
Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.
手鱼际区真实花纹可能属于常染色体显性遗传。
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。
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性眼科疾病,遗传方式有
显性遗传、
隐性遗传和X连锁隐性遗传。
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显性遗传。
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
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
中胚层缺陷。
Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
先天小眼球是一种先天发育异
眼科疾病,
方式有
色体显
、
色体隐
和X连锁隐
。
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
。
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一类
色体隐形
疾病
总称。
声明:以上例句、词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.
摘要牙本质形是一种体染色体显性遗传的中胚层缺陷。
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。
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。
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,部分未经过人工审核,其表达内容亦
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。
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
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。
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。
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。