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    Probe of Screen Standards and Factors on Postpartum Depression
    产后抑郁症的筛查标准及发病因素探讨
    [Methods]From 2003 to 2006,nine hundred newborn babies were investigated by giving a test of BALP,blood serum Calcium,Phosphorous and ALP in order to screen the congenital rickets.
    [方法]2003-2006年,在费县18个乡镇对900名出生1周内的新生儿进行骨碱性磷酸酶(BALP)和血清钙、磷、碱性磷酸酶(ALP)检测,以筛查先天性佝偻病。
    Objective: To screen the mutations of PS-1 gene exon 5-9, discuss the distributing of PS-1 and evaluate its effects on the pathogenesis of AD in Chinese population.
    目的:筛查PS-1基因外显子5~9的突变,了解PS-1基因突变在中国人群中的分布情况及在中国人群阿尔茨海默病(AD)发病中可能产生的影响。
    Objective To establish the methods to detect the nubilous pneumonic cases and to screen out the possible cases infected by SARS, highly pathogenic avian H5N1 virus and other infectious respiratory diseases.
    目的针对不明原因肺炎病例,建立快速、准确的实验室检测方法,及时筛查SARS病毒、高致病性人禽流感H5N1亚型病毒并检测其它亚型流感病毒,呼吸道合胞病毒等病原体,探讨该方法在不明原因肺炎监测中的应用意义。
    Objective To summarize the nursing essentials of hearing screen of high-risk neonates in neonatal intensive care unit (NICU), and to explore the high-risk factors related to hearing disorders.
    目的总结新生儿重症监护室(NICU)中高危新生儿听力筛查的护理要点,探讨与听力异常有关的高危因素。
    Methods:In 252 men with normal spermatogenesis,170 oligospermic and 260 azoospermic patients,we exerted duplex and monoplex PCR technology to screen the deletions of 11 STS sites in AZFc locus and this vicinities. To samples with gr/gr recombinogenic deletion,we applied SFVs method to identify which DAZ gene copies doublet deletion was resulted.
    方法运用单重及多重PCR技术,对252例正常生精男性、430例原发性生精障碍患者(170例原发性少精和260例原发性无精)进行Y染色体AZFc区及其附近的11个序列标签位点(Sequence tagged sites,STS)进行缺失筛查,对发生gr/gr缺失的个体运用SFVs(sequence family variants)法检测DAZ基因拷贝缺失的位置。
    Methods Using National Electronic Disease Surveillance System to output cards and screen for clustered cases, and statistically analyze its effect on reducing disease outbreaks with SPSS 11.5 software.
    方法利用国家疾病监测信息管理系统导出卡片,筛查得出聚集性病例,利用SPSS11.5软件统计分析对降低爆发疫情的作用。
    Objective To screen the polymorphysims of glioma relative gene PLA2G4C with molecular-biological methods and find the relationship between the polymorphysims and pathogenesis of glioma.
    目的运用分子生物学方法筛查脑胶质瘤易感基因PLA2G4C的短串联重复序列的多态性,并进一步确定这些多态性与脑胶质瘤发病的关系。
    Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.
    方法应用地中海贫血一管筛查法和G6PD比值法检测4268对婚前男女的地中海贫血和G6PD缺乏。
    Objective To explore the normality of MOM value of AFP and HCG used to screen the down's syndrome in Jiangsu province , and discuss the feasibility and effectiveness of application of SL transformation in Johnson system of distributions which is used to normalize MOM value of indexes above .
    目的:考察江苏唐氏综合征产前筛查指标AFP和hCG的MoM值的正态性,探索Johnson分布体系中的 SL分布族在上述指标正态性转换中应用的可行性和有效性。
    The analysis of bacterial inhibition method to screen neonatal phenylketonuria in 12 912 infants
    细菌抑制法筛查12912例新生儿苯丙酮尿症结果分析
    Plasma AFP and F-βHCG Tests at Midtrimester of Pregnancy to Screen Down Syndrome
    孕中期血清AFP、F-βHCG筛查唐氏综合征
    PCR-based screen for alpha-thalassemia in Dongguan newborns
    东莞地区新生儿α-地中海贫血的PCR筛查
    The Study of Prenatal Screen for Down Syndrome in Second - trimester by Detecting Maternal Serum Marker.
    孕中期检测母血清标记物筛查唐氏综合征胎儿的研究
    Multicenter study on screen method for gestational diabetes
    妊娠期糖尿病筛查方法的多中心研究
    Study of 8665 cases of the 50 g oral glucose challenge test to screen the gestational diabetes mellitus
    对8665例孕妇行妊娠期糖尿病筛查的临床研究
    The Study of Markers of Serum Pregnancy Using Down Syndrome Screen
    孕母血清标记物在唐氏综合征筛查中的应用
    The evaluation on screen of fever for control of SARS in Beijing
    北京市发热筛查在防控SARS中作用的评价
    A study on the Screen questionnaire of child abuse
    儿童受虐筛查表的效度信度研究
    Plasma AFP and F-HCG tests at midtrfanester of pregnancy to screen Down syndrome
    孕中期血清AFP、F-βHCG筛查唐氏综合征
 

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