A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组、绒毡层组隔维管束异常均是雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒致神经精神障与神经电生理异常的临床表现,提高急性砷中毒在临床工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法体检查排除体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境中氟过量或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

素失禁症是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以中枢神经系统的异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

层组织、绒毡层组织及药隔维管束异常均是雄性因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目探讨急性致神经精神障与神经电生理异常临床表现,提高急性在临床工作认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管疾病，但没有认知异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境氟过量或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及枢神经系统异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均是雄性败育的素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒致经精障与经电生理异常的临床表现,提高急性砷中毒临床工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境中氟过量或乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发生女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢经系统的异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发育畸形有关，少部分放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均是雄性败育因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目探讨急性砷中毒致神经精神障与神经电生理异常临床表现,提高急性砷中毒在临床工作中认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管疾病，但没有认知异常，料暗示了激酶1半合性基因在视觉空间建构认知障中作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境中氟过量或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均是雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒致障与理异常的临床表现,提高急性砷中毒在临床工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量命元素,原环境中氟过量或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢系统的异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠子畸形试验分别检测了乙烯利对小鼠体细胞和殖细胞的致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均是雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒致神经精神障与神经电生理异常的临床表现,提高急性砷中毒在临床工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

是重要微生命元素,原生环境中或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异均是雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒神经精神障与神经电生理异的临床表现,提高急性砷中毒在临床工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异，这些资料暗示了激酶1半合性基因在视觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境中氟过量或缺乏均机体畸变或代谢异。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多与先天性发育畸形有关，少部分因放射治疗后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

层组织、绒毡层组织及药隔维管束是雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷毒致神经精神障与神经电生理的临床表现,提高急性砷毒在临床的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的，这些资料暗示了激酶1半合性基因在视觉空间建构认知障的用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟是重要微量生命元素,原生环境氟过量或缺乏会导致机体畸变或代谢。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及枢神经系统的。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究是运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急砷中毒致神经精神障与神经电生理异常的表现,提高急砷中毒工作中的认识。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采用荧光光度计检测。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合基因视觉空间建构认知障中的作用。

Fluorine is an important trace bio-essential element.Its deficiency or excess related to geological setting can cause organism distortion or supersession abnormality.

氟重要微量生命元素,原生环境中氟过量或缺乏均会导致机体畸变或代谢异常。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症一种罕见的皮肤遗传疾病，通常发生女，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究运用0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者与先天心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数与先天发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。