超声波－蒸汽蒸馏萃取技术富集沉积物样品中的氯代农药和多氯联苯

为方便快速分离沉积物中含氯农药和多氯联苯，将超声波技术和蒸汽蒸馏萃取技术相结合，萃取沉积物中的微量含氯农药和多氯联苯，所得萃取物不需进一步的净化和浓缩，可直接用于色谱分析．实验表明，在进行蒸汽蒸馏萃取之前，使用辅助的超声波技术可将大部分待测物的回收率提高２０％－３０％，较好地解决了由于沉积物的吸附作用而导致的蒸汽蒸馏萃取回收率偏低的缺陷．该法使沉积物样品中的氯代农药和多氯联苯的蒸汽蒸馏萃取富集成为可能．     

Selenium metabolism in animals and humans

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Exencephaly in autosomal dominant brachydactyly syndrome

Exencephaly was diagnosed at 17 weeks in a 27-year-old primigravida with abnormalities of the hands and a family history suggestive of autosomal dominant brachydactyly and clinodactyly. In this family there was also a history of ‘anencephaly’. To our knowledge, this is the first report on the association of exencephaly and autosomal dominant brachydactyly. As the relationship between hand and cranial anomalies is well established, we suggest that this association in our case could be due to a defect in the same gene.     

Triploid fetus: An important consideration in the evaluation of very high maternal serum alpha-fetoprotein

Two patients referred for evaluation of very high maternal serum alpha-fetoprotein (10–20 multiples of the median) were carrying triploid fetuses with placentas showing features of partial hydatidiform mole. The diagnosis of fetal triploidy should be considered when there is a very high maternal serum alpha-fetoprotein and no ultrasound evidence of open neural tube defect, ventral wall defect, or any other explanation. Therefore, chromosomal analysis of amniotic fluid cells in such cases is essential.     

Chorionic villus sampling: Improved method for preparation of karyotypes after short-term incubation

A method for the isolation and trypsin-Giemsa banding of metaphases obtained after short-term incubation (48 h) of cytotrophoblast cells from chorionic villus sample is described. A new slide-making instrument, developed expressly to enhance the spreading of chromosomes from metaphases released from small tissue pieces, is responsible for the increase yield of analysable metaphases in this protocol.     

Experimentally proved biosynthesis of vitamin C in a guinea pig

The Science of Nature -     

Prenatal diagnosis of pericentric inversion of chromosome no. 17 in a twin pregnancy

Although prenatal genetic diagnosis can usually provide prospective parents with information as to whether their fetus is affected with certain genetic conditions, the presence of twins and the uncertainty about the phenotype of some chromosome variations pose a major dilemma and make genetic counselling very difficult. Here, a case report of an unusual chromosome aberration (pericentric inversion of chromosome no. 17) in a twin pregnancy which was originally suspected to be monoamniotic but later proved to have two sacs was presented.