Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子产量低，育苗、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横耳家系的临床表现遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家系统—RIMER专家系统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子，育苗、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目鉴定一痒疹样营养不良型大疱性表皮松解症家系基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳家系临床表现及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等、可捕进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理置信规则库推理方法(RIMER)已被提出,由此生了一种新型专家系统—RIMER专家系统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性种子产量低，育苗、造林时这些容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他成员除一名为先天性耳聋外, 均为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性皮松解症的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳的临床及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专—RIMER专。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子产量低，育苗、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附家系的临床表现及遗传。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家系统—RIMER专家系统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子产量，、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目鉴定一痒疹样营养不良型大疱性表皮松解症家系基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳家系临床表现及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家系统—RIMER专家系统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性种子产量低，育苗、造林时这些家容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳家的临床表现及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家统可以对要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家统—RIMER专家统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子产量低，育苗、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性耳, 表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳家系的临床表现及遗征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家系统—RIMER专家系统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性种子产量低，育苗、造林时这容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他成员除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症的基突变,为进一步开展基诊断和基治疗奠定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳的临床表现及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专统可以对东海主要经济种类,如带、和马面屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专统—RIMER专统。

Production of some clonally seeds were low, these lines were easy to be lost while planting.

由于部分无性系种子产量低，育苗、造林时这些家系容易丢失。

The proband exhibits congenital severe sensorineural hearing loss, heterochromia iridis and facial freckles.

其他家系成员除一名仅表现为先天性耳聋外, 均表现为颜面、上肢雀斑和/或早白发。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹不良型大疱性表皮松解症家系的基突变,为进一步开展基诊断和基定基础。

Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.

分析1组面横裂及附耳家系的临床表现及遗传学特征。

The stock sizes and catchable yields for hairtail, chub mackerel and filefish in the East China Sea can be estimated by the expert system.

运用该专家系统可以对东海主要经济种类,如带鱼、鲐鱼和马面鱼屯等的资源量、可捕量进行评估和预报。

A belief rule -base inference methodology using the evidential reasoning approach (RIMER) has been developed, the RIMER expert system is explored on the basis of RIMER.

基于证据推理的置信规则库推理方法(RIMER)已被提出,由此产生了一种新型专家系统—RIMER专家系统。