全文获取类型
收费全文 | 31390篇 |
免费 | 4526篇 |
国内免费 | 26581篇 |
专业分类
安全科学 | 1535篇 |
废物处理 | 1216篇 |
环保管理 | 3753篇 |
综合类 | 32317篇 |
基础理论 | 8775篇 |
环境理论 | 10篇 |
污染及防治 | 10685篇 |
评价与监测 | 2779篇 |
社会与环境 | 1066篇 |
灾害及防治 | 361篇 |
出版年
2021年 | 148篇 |
2020年 | 702篇 |
2019年 | 1977篇 |
2018年 | 2350篇 |
2017年 | 2346篇 |
2016年 | 2306篇 |
2015年 | 2544篇 |
2014年 | 3292篇 |
2013年 | 4532篇 |
2012年 | 3800篇 |
2011年 | 3356篇 |
2010年 | 2853篇 |
2009年 | 2818篇 |
2008年 | 2638篇 |
2007年 | 2713篇 |
2006年 | 2090篇 |
2005年 | 2001篇 |
2004年 | 2017篇 |
2003年 | 1671篇 |
2002年 | 1179篇 |
2001年 | 1364篇 |
2000年 | 1245篇 |
1999年 | 923篇 |
1998年 | 703篇 |
1997年 | 696篇 |
1996年 | 732篇 |
1995年 | 732篇 |
1994年 | 553篇 |
1993年 | 478篇 |
1992年 | 538篇 |
1991年 | 535篇 |
1990年 | 522篇 |
1989年 | 474篇 |
1988年 | 391篇 |
1987年 | 310篇 |
1986年 | 291篇 |
1985年 | 255篇 |
1984年 | 308篇 |
1983年 | 250篇 |
1982年 | 318篇 |
1981年 | 254篇 |
1980年 | 186篇 |
1979年 | 205篇 |
1978年 | 190篇 |
1977年 | 156篇 |
1975年 | 145篇 |
1974年 | 161篇 |
1973年 | 162篇 |
1972年 | 153篇 |
1971年 | 150篇 |
排序方式: 共有10000条查询结果,搜索用时 41 毫秒
811.
812.
Epidemiological survey of 573 families, clinical examination of 2593 persons, and X-ray examination of 1136 persons (in 16 typical endemic villages) were conducted, based on the classification of endemiology for KBD disease areas, i.e, mountain type, loess plateau type, plateau type, and flatlands type. It was revealed that the KBD disease areas exhibited the regular pattern of corming-into-being, development and passing-away and the characteristics of growth and decline. Further, it was found clinically that the disease areas may be divided into 4 types, i.e., recent onset, developing, stable, and historical. This division is simple and easy, practical, scientific, and reliable and can be applied by medical personnel at different levels. 相似文献
813.
This paper discusses the scientific background and content of the ecological assessment of cities, and takes Boda, a new town in Xinjiang province, China, as a case study. 相似文献
814.
Arie Drugan Anne Greb Mark Paul Johnson Eric L. Krivchenia Wendy R. Uhlmann Kamran S. Moghissi Mark I. Evans MD 《黑龙江环境通报》1990,10(8):483-490
Parental decisions concerning the continuation of pregnancy following prenatal detection of abnormal chromosomes were evaluated for 80 patients whose diagnosis and prenatal counselling were performed in our centre. Twenty-two anomalies were diagnosed by chorionic villus sampling (CVS) and 58 by amniocentesis. The severity of the chromosome anomaly and associated ultrasound findings in the first vs. second trimester were correlated with patients' decisions. No difference was found in the likelihood of parental decisions to interrupt or continue a pregnancy between CVS and amniocentesis for either the‘severe’ or the‘questionable’ group of chromosome anomalies. Ninety-three per cent of patients with severe prognosis and 27 per cent with questionable prognosis opted for pregnancy termination (p <0·0001). The association of ultrasound anomalies and termination was highly significant (p< 0·001). The severity of the chromosome anomaly, and, to a lesser extent, the visualization of anomalies on ultrasound were the major determinants of parental decisions to terminate the pregnancy. The diagnosis of an anomaly in the first trimester was no more likely ito lead to a termination of pregnancy than in the second trimester. 相似文献
815.
William D. Boelter MD Beth Ann Burt Elaine B. Spector David R. Hinton Zdena Pavlova Atsuko Fujimoto 《黑龙江环境通报》1990,10(11):703-715
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. 相似文献
816.
817.
818.
819.
820.