咨询与建议

限定检索结果

文献类型

  • 79 篇 期刊文献
  • 12 篇 会议
  • 1 册 图书
  • 1 篇 学位论文

馆藏范围

  • 93 篇 电子文献
  • 0 种 纸本馆藏

日期分布

学科分类号

  • 81 篇 医学
    • 77 篇 临床医学
    • 9 篇 医学技术(可授医学...
    • 1 篇 基础医学(可授医学...
    • 1 篇 公共卫生与预防医...
    • 1 篇 中西医结合
  • 14 篇 理学
    • 12 篇 生物学
    • 1 篇 数学
    • 1 篇 统计学(可授理学、...
  • 13 篇 工学
    • 6 篇 生物医学工程(可授...
    • 5 篇 生物工程
    • 2 篇 化学工程与技术
    • 1 篇 计算机科学与技术...
    • 1 篇 环境科学与工程(可...
    • 1 篇 软件工程
  • 6 篇 农学
    • 6 篇 作物学
    • 1 篇 植物保护
  • 1 篇 经济学
    • 1 篇 应用经济学
  • 1 篇 文学
    • 1 篇 外国语言文学

主题

  • 93 篇 prenatal diagnos...
  • 9 篇 case report
  • 6 篇 amniocentesis
  • 5 篇 ultrasound
  • 5 篇 mutation
  • 3 篇 genetic counseli...
  • 3 篇 ultrasonography
  • 3 篇 fetus
  • 3 篇 chorionic villus...
  • 3 篇 echocardiography
  • 2 篇 magnetic resonan...
  • 2 篇 whole exome sequ...
  • 2 篇 pregnancy outcom...
  • 2 篇 fetal ultrasound
  • 2 篇 aneuploidy
  • 2 篇 fetal echocardio...
  • 2 篇 copy number vari...
  • 2 篇 three dimension...
  • 2 篇 non-invasive pre...
  • 2 篇 congenital heart...

机构

  • 3 篇 department of ob...
  • 2 篇 department of ob...
  • 2 篇 key laboratory f...
  • 2 篇 department of me...
  • 2 篇 浙江大学医学院附...
  • 1 篇 department of pa...
  • 1 篇 department of ob...
  • 1 篇 chinese academy ...
  • 1 篇 prenatal diagnos...
  • 1 篇 neonatal departm...
  • 1 篇 department of ul...
  • 1 篇 department of or...
  • 1 篇 department of ge...
  • 1 篇 NOT FOUND
  • 1 篇 department of or...
  • 1 篇 prenatal diagnos...
  • 1 篇 department of pe...
  • 1 篇 comprehensive ge...
  • 1 篇 department of ob...
  • 1 篇 department of pe...

作者

  • 2 篇 许建平
  • 2 篇 shi chun-yan
  • 2 篇 preethi navaneet...
  • 2 篇 张铭
  • 2 篇 yongyi ma
  • 2 篇 jianxia huang
  • 2 篇 sumita danda
  • 2 篇 jin mei
  • 2 篇 yiming chen
  • 2 篇 徐辉雄
  • 2 篇 杨建滨
  • 2 篇 min chen
  • 2 篇 张青萍
  • 2 篇 zhu hai-yan
  • 2 篇 肖先桃
  • 2 篇 manisha m.beck
  • 2 篇 hong yao
  • 2 篇 闻良珍
  • 2 篇 陈汉平
  • 2 篇 郑树

语言

  • 59 篇 英文
  • 34 篇 中文
检索条件"主题词=prenatal diagnosis"
93 条 记 录,以下是1-10 订阅
排序:
prenatal diagnosis of choledochal cyst using magnetic resonance imaging: A case report
收藏 引用
World Journal of Gastroenterology 2005年 第32期11卷 5082-5083页
作者: Alex Mun-Ching Wong Yun-Chung Cheung Yu-Hung Liu Koon-Kwan Ng Siu-Cheung Chan Shu-Hang Ng Department of Diagnostic RadiologyChang Gung Memorial Hospital Kwei-ShanTao-YuanTaiwanChina Obstetrics and GynecologyChang Gung Memorial Hospital 222Mei Chin RoadKeelungTaiwanChina
Choledochal cysts are congenital anomalies of the biliary ducts, characterized by cystic dilatation of the *** diagnosis of this anomaly using ultrasonography (US) has been well documented. Magnetic resonance imaging ... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
prenatal diagnosis of spinocerebellar ataxia type 3/Machado-Joseph disease in China's Mainland A case report
收藏 引用
Neural Regeneration Research 2011年 第26期6卷 2047-2049页
作者: Lifang Lei Junling Wang Shen Zhang Hong Jiang Lu Shen Qian Xu Xinxiang Yan Yi Yuan Qian Pan Kun Xia Beisha Tang Department of Neurology Xiangya Hospital Central South University Changsha 410008 Hunan Province China Department of Neurology Xian-gya Third Hospital Central South University -Changsha 410013 Hunan Province China National Laboratory of Medical Genetics of China Changsha 410008 Hunan Province China
Spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is a progressive, currently untreatable and ultimately fatal ataxic disorder that belongs to the group of neurological disorders known as CAG-repeat or... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
prenatal diagnosis of triphalangeal thumb-polysyndactyly syndrome by ultrasonography combined with genetic testing:A case report
收藏 引用
World Journal of Clinical Cases 2021年 第23期9卷 6832-6838页
作者: Shi-Jie Zhang Hai-Bin Lin Qiu-Xia Jiang Shao-Zheng He Guo-Rong Lyu Department of Ultrasound The Second Affiliated Hospital of Fujian Medical UniversityQuanzhou 362000Fujian ProvinceChina Department of Ultrasound Jinjiang Municipal HospitalQuanzhou 362000Fujian ProvinceChina Department of Ultrasound Quanzhou Women’s and Children’s HospitalQuanzhou 362000Fujian ProvinceChina Collaborative Innovation Center for Maternal and Infant Health Service Application Technology of Education MinistryQuanzhou Medical CollegeQuanzhou 362000Fujian ProvinceChina
BACKGROUND Triphalangeal thumb-polysyndactyly syndrome(TPT-PS)is a rare type of congenital limb deformity,and most studies focus on the *** reports of the sonographic characteristics of TPT-PS during pregnancy are ***... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
prenatal diagnosis of an Apically Located Congenital Left Ventricular Aneurysm: A Rare Case
收藏 引用
Congenital Heart Disease 2024年 第1期19卷 123-129页
作者: Yücel Kaya And Yavuz Hasan Berkan Sayal Büşra Tsakir Gökalp Kabacaoğlu Kadriye NilayÖzcan Department of Perinatology Antalya Education and Research HospitalUniversity of Health SciencesAntalyaTurkey Department of Perinatology Faculty of MedicineSüleyman Demirel UniversityIspartaTurkey
Congenital ventricular aneurysm is a very rare cardiac anomaly.A diagnosis can be made during the prenatal period using fetal *** study presents a very rare apically located left ventricular aneurysm case,and the rele... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
prenatal diagnosis of isolated lateral facial cleft by ultrasonography and three-dimensional printing:A case report
收藏 引用
World Journal of Clinical Cases 2021年 第24期9卷 7196-7204页
作者: Wen-Ling Song Hai-Ou Ma Yu Nan Yu-Jia Li Na Qi Li-Ying Zhang Xin Xu Yuan-Yi Wang Department of Obstetrics The First Hospital of Jilin UniversityChangchun 130021Jilin ProvinceChina prenatal diagnosis Center The Second Hospital of Jilin UniversityChangchun 130021Jilin ProvinceChina Department of Spine Surgery The First Hospital of Jilin UniversityJilin Engineering Research Center for Spine and Spinal CordChangchun 130021Jilin ProvinceChina
BACKGROUND Lateral facial clefts are atypical with a low incidence in the facial cleft *** the development of ultrasonography(US)prenatal screening,such facial malformations can be detected and diagnosed prenatally ra... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
prenatal diagnosis of cor triatriatum sinister associated with early pericardial effusion:A case report
收藏 引用
World Journal of Clinical Cases 2021年 第17期9卷 4395-4399页
作者: Esther Cánovas Eduardo Cazorla Melanie Cristine Alonzo Rebeca Jara LeyreÁlvarez Duska Beric Department of Obstetrics and Gynecology University Hospital of TorreviejaAlicante 03186Spain
BACKGROUND Cor triatriatum sinistrum or cor triatriatum sinister is a rare congenital heart disease that accounts for approximately 0.1%of all cardiac *** is defined as the presence of an anomalous septum that divides... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss
收藏 引用
Journal of Genetics and Genomics 2010年 第12期37卷 787-793页
作者: Jianzhong Li Jing Cheng Yanping Lu Yu Lu Airing Chen YiSun Dongyang Kang Xin Zhang Pu Dai Dongyi Han Huijun Yuan Institute of Otolaryngology Chinese PLA General Hospital Beijing 100853 China Department of Otolaryngology Fuzhou General Hospital of Nanjing Command PLA Fuzhou 350025 China Department of Obstetrics and Gynecology General Hospital of PLA Beijing 100853 China
We present the clinical and genetic findings for a Chinese family with X-linked non-syndromic hearing loss in which the affected males showed congenital profound sensorineural hearing impairment. In two affected broth... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
Enrichment of Fetal Nucleated Red Blood Cells by Multi-core Magnetic Composite Particles for Non-invasive prenatal diagnosis
收藏 引用
Chemical Research in Chinese Universities 2012年 第3期28卷 443-448页
作者: PAN Ying WANG Qing HUANG Wen-jun QIAO Feng-1i LIU Yu-ping ZHANG Yu-cheng HAI De-yang DU Ying,ting WANG Wen-yue ZHANG Ai-chen Department of Gynaecology and Obstetrics China-Japan Union HospitalJilin UniversityChangchun 130033P.R.China Department of Endocrine China-Japan Union HospitalJilin UniversityChangchun 130033P.R.China Department of Transfusion the Second Hospital of Jilin UniversityChangchun 130041P R.China Department of Electric Diagnose Central Laboratory China-Japan Union HospitalJilin UniversityChangchun 130033P.R.China
A novel kind of multi-core magnetic composite particles, the surfaces of which were respectively mo- dified with goat-anti-mouse IgG and antitransferrin receptor(anti-CD71), was prepared. The fetal nucleated red blo... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
Population-based carrier screening and prenatal diagnosis of fragile X syndrome in East Asian populations
收藏 引用
Journal of Genetics and Genomics 2021年 第12期48卷 1104-1110页
作者: Qiwei Guo Yih-Yuan Chang Chien-Hao Huang Yu-Shan Hsiao Yu-Chiao Hsiao I-Fan Chiu Yulin Zhou Haixia Zhang Tsang-Ming Ko United Diagnostic and Research Center for Clinical Genetics Women and Children's HospitalSchool of Medicine&School of Public HealthXiamen UniversityXiamenFujian 361102China Genephile Bioscience Laboratory Ko's Obstetrics and GynecologyTaipei 100TaiwanChina Biofast Biotechnology Co. Ltd.XiamenFujian 361102China
Identification of carriers of fragile X syndrome(FXS) with the subsequent prenatal diagnosis and knowledge of FXS-associated genetic profiles are essential for intervention in specific populations. We report the resul... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论
Clinical manifestations and prenatal diagnosis of Ullrich congenital muscular dystrophy: A case report
收藏 引用
World Journal of Clinical Cases 2022年 第1期10卷 338-344页
作者: Jun Hu Yan-Hui Chen Xin Fang Yu Zhou Feng Chen Department of Pediatrics Fujian Medical University Union HospitalFuzhou 350001Fujian ProvinceChina Department of Obstetrics and Gynecology Fujian Medical University Union HospitalFuzhou 350001Fujian ProvinceChina Department of Pediatric Surgery Fujian Medical University Union HospitalFuzhou 350001Fujian ProvinceChina
BACKGROUND Ullrich congenital muscular dystrophy(UCMD)is one of the collagen-VI-related myopathies caused by mutations of COL6A1,COL6A2,and COL6A3 *** individuals are characterized by muscle weakness,proximal joint co... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论