Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属色体隐性病。

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.

先天性小球是一种先天发育异性科疾病,方式有色体显性、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.

肤白化病是由黑色素合成相关基因突变导致、肤、毛发黑色素沉着减少或缺乏引起的一类色体隐形疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传病。

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

手际区真实花纹可能属于常染色体显性传。

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

先天性眼球是一种先天发育异常性眼科疾病,传方式有常染色体显性传、常染色体隐性传和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相关基因突变导致眼、皮肤、毛发黑色沉着减少或缺乏引起的一类常染色体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染传病。

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,传方式有常染传、常染传和X连锁传。

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形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性。

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,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的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传病。

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,传方式有常染色体显性传、常染色体隐性传和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、毛发黑色素沉着减乏引起的一类常染色体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传病。

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,传方式有常染色体显性传、常染色体隐性传和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的一类常染色体隐形传疾病的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性传。

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

手掌小鱼际区真可能属于常染色体显性传。

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

先天性小眼球一种先天发育异常性眼科疾,传方式有常染色体显性传、常染色体隐性传和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的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于常染色体隐性。

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,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的总称。

Maple tree saccharorrhea sickness belongs to the euchromosome recessive hereditary disease.

枫糖尿症属于体隐传病。

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眼科疾病,传方式有体显传、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传疾病的总称。