Prenatal diagnosis of 21-hydroxylase deficiency by rflp analysis of the 21-hydroxylase,complement C4, and HLA class II genes

In 19 pregnancies at risk for 21-hydroxylase deficiency (21OHD) in 18 families with at lea one affected child, prenatal diagnosis was performed by RFLP analysis using the enzymi Taq I and EcoRI and the DNA probes specific for the 21 OH genes, the closely linke complement C4 genes and the highly polymorphic HLA class II genes DRB, DQB, and DPI For fetal DNA analysis either chorionic villi or cultivated amniotic cells were used. In all 1 cases, a clear prenatal diagnosis was possible either with the 21OH probe alone or in mo cases, by combining the results of the different closely linked loci.     

Dystrophin protein and rflp analyis for fetal diagnosis and carrier confirmation of duchenne muscular dystrophy

A pregnant woman with indeterminate Duchenne muscular dystrophy (DMD) carrier status, but with DMD diagnosed in her deceased brother (unavailable for study), presented for prenatal diagnosis, intending to continue the pregnancy only if proven unaffected with DMD with near absolute certainty. Creatine kinase (CK) assays to clarify carrier status were inconclusive. Male sex in the fetus was identified, but DNA restriction fragment length polymorphism (RFLP) analysis was not yet available to this centre to investigate the possible transmission of the DMD gene, and the pregnancy was terminated. Tissue histology and dystrophin protein analysis demonstrated the absence of DMD. In a situation with proven maternal carrier status, future fetal inheritance of the opposite maternal X chromosome would indicate the presence of DMD. However, maternal carrier status remained in doubt through a second pregnancy, even with RFLP studies, and was finally established when dystrophin analysis confirmed the presence of DMD in the second fetus. Histologic findings are presented, contrasting features in the two fetuses. The value of dystrophin analysis for establishing the diagnosis of fetal DMD, in this case proving maternal carrier status in a difficult situation, and for demonstrating DMD gene:RFLP haplotype relationships is illustrated.     

锅炉除尘脱硫及其废水回用系统的经济损益分析

以燃煤锅炉掺烧固硫除尘脱硫及其废水回用系统为研究对象，利用环境系统费用效益分析方法，分析了该系统的环保投入和取得的环境效益。结果表明：对燃烧高硫煤的８０ｔ／ｈ规模的锅炉房，环保费用的现值为３１２６万元，环保效益的现值为９７２９万元，费用与效益之比为１∶３１１。结果说明锅炉掺烧固硫除尘脱硫及其废水循环技术具有很好的经济效益。该分析方法和结果为燃煤锅炉除尘脱硫工艺方案的选择和系统的优化研究提供了基础。     

量纲分析对污水近区初始稀释度变化规律的探讨

在上海合流污水二期工程白龙港排放口水力模型试验基础上，根据模型实验的大量数据，采用量纲分析方法对近区初始稀释度的变化规律进行了探讨，得出了描述该区域初始稀释度变化规律的半理论半经验公式，可为实际排海工程的设计提供依据。     

色谱痕量分析中的非线性效应及影响

根据溶质在流动相与固定相中吸附平衡热力学的观点简要讨论了色谱分离中的非线性原理，及其在进行色谱痕量分析采用大进样量时对定性和定量的影响，并提出了改进方法。同时也探讨了非线性效应对样品前处理及未知物馏份制备分离的影响与应用。     

催化动力学光度法测定痕量铈

根据前量铈在稀硫酸介质中对重铬酸根氧化ＥＤＴＡ而褪色的反应有催化作用，建立了测定痕量铈的新动力学光度法，测定范围为０￣２．４×１０＾－２μｇ／ｍＬ，检限限为５．２×１０＾－１０ｇ／ｍＬ，用于测定人发中的痕量铈，结果满意。     

住宅小区中水回用系统经济技术分析

中水回用作为一项保护环境、节约资源的措施,将有力地促进城市的可持续发展和加速生态城市的建设,是解决中国水资源危机的有效途径之一.文章着重对住宅小区的中水回用系统进行了经济技术分析.     

燃烧型煤排放可吸入尘中的成分分析

主要运用X 射线荧光光谱的半定量分析方法 ,测量了民用炉灶燃烧型煤排放的可吸入尘中的主要成分 ,从而得出在可吸入尘中的主要元素为Cl、S、Na、K ,并研究了其产生的原因     

Environmental input-output model and its analysis with a focus on the solid waste management sectors

ＩｎｔｒｏｄｕｃｔｉｏｎＳｉｎｃｅｔｈｅｆｉｒｓｔｅｎｖｉｒｏｎｍｅｎｔａｌｉｎｐｕｔｏｕｔｐｕｔｍｏｄｅｌ(ＥＩＯＭ)(Ｃｕｍｂｅｒｌａｎｄ,1966)ｗａｓｅｓｔａｂｌｉｓｈｅｄｂｙｉｎｃｏｒｐｏｒａｔｉｎｇｅｎｖｉｒｏｎｍｅｎｔａｌｆａｃｔｏｒｓｉｎｔ?..     

Neutron activation method in the analysis of environmental objects

ＮｅｕｔｒｏｎａｃｔｉｖａｔｉｏｎｍｅｔｈｏｄｉｎｔｈｅａｎａｌｙｓｉｓｏｆｅｎｖｉｒｏｎｍｅｎｔａｌｏｂｊｅｃｔｓＧ．Ｍ．Ｋｏｌｅｓｏｖ（Ｖ．Ｉ．ＶｅｒｎａｄｓｋｙＩｎｓｔｉｔｕｔｅｏｆＧｅｏｃｈｅｍ。＆Ａｎａｌ．Ｃｈｅｍ．，ＲｕｓｓｉａｎＡｃａｄ...