首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   33453篇
  免费   675篇
  国内免费   1487篇
安全科学   1161篇
废物处理   1255篇
环保管理   4395篇
综合类   7005篇
基础理论   9232篇
环境理论   21篇
污染及防治   8806篇
评价与监测   2007篇
社会与环境   1414篇
灾害及防治   319篇
  2023年   196篇
  2022年   375篇
  2021年   365篇
  2020年   339篇
  2019年   363篇
  2018年   560篇
  2017年   577篇
  2016年   736篇
  2015年   679篇
  2014年   967篇
  2013年   2543篇
  2012年   1203篇
  2011年   1604篇
  2010年   1327篇
  2009年   1348篇
  2008年   1541篇
  2007年   1588篇
  2006年   1416篇
  2005年   1191篇
  2004年   1118篇
  2003年   1090篇
  2002年   1044篇
  2001年   1324篇
  2000年   953篇
  1999年   623篇
  1998年   504篇
  1997年   493篇
  1996年   505篇
  1995年   528篇
  1994年   470篇
  1993年   422篇
  1992年   447篇
  1991年   384篇
  1990年   392篇
  1989年   419篇
  1988年   350篇
  1987年   305篇
  1986年   280篇
  1985年   312篇
  1984年   288篇
  1983年   323篇
  1982年   323篇
  1981年   275篇
  1980年   244篇
  1979年   271篇
  1978年   229篇
  1977年   195篇
  1976年   201篇
  1975年   192篇
  1972年   199篇
排序方式: 共有10000条查询结果,搜索用时 750 毫秒
501.
502.
503.
504.
505.
We report two cases of apparently balanced complex de novo chromosomal rearrangements (BCCR) detected prenatally at 17 weeks and 10 weeks of gestation, respectively. Chromosomes were studied using GTG-banding and fluorescent in situ hybridization (FISH). In one case four chromosomes and in the other case three chromosomes were involved in the rearrangements. One of the pregnancies was terminated and no external or internal abnormalities were detected at autopsy. The other pregnancy continued to term. Level III ultrasound examination showed no abnormalities. The child is now 3 years old and has neither congenital anomalies nor evidence of delayed psychomotor development.  相似文献   
506.
A prenatally detected case of a rare mosaic tetrasomy 12p/trisomy 12p is reported, presenting as the well-known accessory isochromosome 12p and a supernumerary single 12p marker in 17/24 and 6/24 clones of cultured amniotic fluid cells, respectively. The chromosomal nature of both marker chromosomes was investigated in cultured amniotic fluid cells by fluorescent in situ hybridization with various probes: the 12-centromeric probes pa12H8 and D12Z3, a whole chromosome 12 paint, and the chromosome 12p-specific paint M28. DNA analysis revealed a maternal origin of the extra 12p material. After counselling, the parents requested termination of pregnancy. Inspection and autopsy of the fetus revealed many of the dysmorphisms and internal structural abnormalities of the Pallister–Killian syndrome.  相似文献   
507.
In a case of hydrops fetalis, serological examination showed a recent maternal human parvovirus B19 infection. Amniocentesis revealed a unique unbalanced translocation between chromosomes 3 and 11 of the fetus. The mother proved to have a balanced reciprocal translocation between chromosomes 3 and 11. A grossly macerated hydropic male fetus was delivered with a flat nose and low implanted deformed ears. Histopathological examination revealed nuclear inclusion bodies in fetal erythroid cells, confirming human parvovirus B19 infection. Parvovirus B19 DNA was demonstrated by in situ hybridization in the nuclei of heart muscle cells. Our finding of two different disorders in one case illustrates the importance of a complete evaluation of every case of hydrops fetalis, especially concerning counselling on the outcome of future pregnancies. The human parvovirus B19 infection will not recur due to the acquired immunity of the mother, whereas the balanced reciprocal translocation will endanger future pregnancies.  相似文献   
508.
A 17-year-old woman was referred for amniocentesis due to a low maternal serum alpha-fetoprotein (AFP) concentration in a voluntary screening test. The fetal karyotype was 48,XXYY, and the pregnancy was terminated. Autopsy of the fetus disclosed agenesis of the corpus callosum and unusual facial features.  相似文献   
509.
A simplified method is described for processing both direct preparations and long-term cultures from the same fragment of chorionic villi. Enzyme separation of the outer trophoblast layers (used for direct preparations) from the inner mesenchymal core (used to initiate long-term cultures) facilitates the utilization of the same fragments for the two procedures, without jeopardizing the success of either method. This has proved useful in cases where the sample was so small that only one method of chromosome preparation may have been possible using other techniques.  相似文献   
510.
采用活性炭管吸附大气中基苯乙烯,以二硫化碳洗脱,以溴水加成后,用气相色谱电子捕获器测定苯乙烯的二溴加成物。本方法适合于检测多种污染物共存的大气中痕量苯乙烯。其线性范围为0.015-0.74ng,最低检出浓度为0.001mg/m^3;重现性实验的变异系数为2.3%:当活性炭管吸附苯乙烯在2.9μg时,回收率为90%,吸附苯乙烯0.29μg时,回收率为72%。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号