Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探解决颧骨过高和颏部短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨短小和双脚内旋，有面部小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它真正的**短小完全不，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒症其特点为短小的四肢、小胸、巨头及脑部发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的人上发现，这发现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏部短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨短小和双脚内旋，同时有面部小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒其特点为短小的四肢、小胸、巨头及脑部发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的病人上发现，这些病例发现都属于一种特殊遗群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨和双脚内旋，同时有面颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**完全不同，后者有一个冷的医学名称：**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒症其特点为的四肢、胸、巨头及脑发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在的病人上发现，这些病例发现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所侧股骨短小和脚内旋，同时有面小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常的致死性新生儿侏儒症其特点短小的四肢、小胸、巨头发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的病人上发现，这些病例发现都属于一种特殊遗传症候群-第十四母体单亲染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧和颏部短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股短小和双脚内旋，同时有面部小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒症其特点为短小的四肢、小胸、巨头及脑部发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的发现，这些例发现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏部短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）所见为双侧股骨短小和双脚内旋，同时有面部小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒症其特点为短小的四肢、小胸、巨头及脑部常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的病人上现，这些病例现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏部的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨和双脚内旋，同时有面部颌和平额形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**全不同，后者有一个冷的医学名称：**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死是最常见的致死新生儿侏儒症其特点为的四肢、胸、巨头及脑部发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材的病人上发现，这些病例发现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏部短小的一新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨短小和双脚内旋，同时有面部小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏儒症其点为短小的四肢、小胸、巨头及脑部发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的病人上发现，这些病例发现都属于一遗传症候群-第十四母体单亲双染色体。

Objective To improve the effect of operation for patients with prominent malar complex and microgenia.

探讨同时解决颧骨过高和颏短小的一种新方法。

The findings are bilateral short femurs and endorotation of both feet.There is also discrete facial dysmorphism with micrognathia and flat forehead.

（超声）检查所见为双侧股骨短小和双脚内旋，同时有小颌和平额畸形。

It's a totally different condition from haing a truly tiny tinkler, a condition known by the cold, clinical name of micropenis.

它同真正的**短小完全不同，后者有一个冷的医学名称：小**。

Thanatophoric dysplasia (TD) is the most common form of lethal neonatal dwarfism with micromelic shortening of the limbs, macrocephaly, platyspondyly, and reduced thoracic cavity.

摘要致死性畸胎是最常见的致死性新生儿侏特点为短小的四肢、小胸、巨头及脑发育异常等。

14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小的病人上发现，这些病例发现都属于一种特殊遗传候群-第十四母体单亲双染色体。