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染色显性传中胚层缺。

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

手小鱼际区真实花纹可能属于常染色显性传。

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,传方式有常染色显性传、常染色隐性传和X连锁隐性传。

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一类常染色隐形传疾病总称。

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.

先天性是一种先天发育异常性科疾病,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.

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的一类常染色体隐形遗传疾病的总称。

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传。

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常眼科疾病,传方式有常染色体传、常染色体隐传和X连锁隐传。

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传疾病的总称。

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

摘要牙本质形成不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.

天性小眼球种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类常染色体隐形遗传疾病的总称。

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.

手掌鱼际区真实花纹可能属于常染色体显遗传。

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

先眼球是一种先发育异常眼科疾病,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。

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。

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,遗有常色体显性遗、常色体隐性遗和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色体隐形遗疾病的总称。

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。

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传。

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常眼科疾病,传方式有常染色体传、常染色体隐传和X连锁隐传。

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传疾病的总称。

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性眼科疾病,遗传方有染色体显性遗传、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、毛发黑色素沉着减少或缺乏引起的一类染色体隐形遗传疾病的总称。