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.     

试论我国环境行政强制执行制度

环境行政强制执行制度是环境执法的重要制度。大陆法系国家实行德奥模式而从法律上确立环境行政机关强制执行地位，英美法系国家一般实行美法模式而以诉讼方式实现环境行政强制执行，日本则有更为严格、完善的环境行政强制执行制度。比较上述模式后认为：基于我国国情，法律应赋予环境行政机关一定的直接强制执行权，明确环境行政强制执行与司法强制执行的权限，确立环境行政强制执行制度。     

反气相色谱法测定麦饭石对苯类的吸附

以麦饭石为吸附质，采用反气相色谱法测定了载气流量、麦饭石装柱质量和载气湿度对吸附等温线测定的影响，测定了苯等４种挥发性芳香类有机物在麦饭石颗粒上的吸附焓。结果表明，在水蒸汽存在的条件下，苯等４种挥发性有机物在麦饭石颗粒上的吸附能遵循理想气相色谱方程，且测得的吸附焓和其蒸发焓较接近。     

磷肥厂副产氟硅酸利用的新方法

以磷肥厂副产氟硅酸为原料 ,加上碳酸钠 ,在适宜的工艺条件下反应 ,制取符合GB42 93— 84一级品的氟化钠和符合GB10 5 71— 89的白炭黑。该工艺具有原料易得、能耗低、成本低、投资省、无污染、经济效益好等优点     

关于环境自动监测的系统设计和方案探讨

根据上海市环境监测的现状，分别从大气环境、污染源排放、水和废水监测等方面提出了进一步开展自动监测的设想和网络优化设计，并探讨了有关管理措施。     

火电厂烟气脱硫工艺国产化初探

火电厂排放的SO2形成酸雨已严重危害人类生存环境。国家把解决烟气脱硫问题纳入大政方针之中，强制要求火电厂必须安装烟气脱硫装置。文章介绍了几种目前国际上较为成熟的脱硫工艺，并对各种工艺进行了比较，分析了国内烟气脱硫市场，并就脱硫技术国产化问题提出若干看法。     

广东省危险废物处置设施与管理现状及对策

文章对广东省危险废物的产生与流向、处置设施建设、工艺技术、污染防治以及管理等现状及存在问题进行调查分析，针对所存在的问题，并结合规划要求，从管理、技术发展、处理处置设施建设和运营等方面提出较为系统的危险废物污染防治对策。     

太阳光助Fenton体系氧化降解苯酚废水的研究

探讨了太阳光助Fenton体系对苯酚的氧化降解。结果表明，太阳光能有效地增强Fenton试剂对苯酚的氧化降解，在晴天较强太阳光照下，Fenton试剂可在较短时间内使较高浓度的苯酚完全矿化。反应体系的初始pH值及Fe^2 用量均对苯酚的氧化降解有明显影响，反应的适宜pH值在3—4的酸性范围内；适量Fe^2 参与的太阳光—Fenton反应有助于苯酚的降解，但过高的Fe^2 用量反而不利于苯酚的降解。实验结果还表明，采用分批多次投加的方式可明显提高氧化剂H202的利用效率，降低H202的消耗量；苯酚废水降解的主要中间产物为苯醌和有机酸；一定程度的太阳光—Fenton预氧化处理可使废水的BOD5／C02cr比值由0.10捉高到0.32，可生化性明显提高。