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排序方式: 共有10000条查询结果,搜索用时 31 毫秒
281.
Dr. C. Dawn DeLozier-Blanchet Eric Engel Philippe Extermann Béatrice Pastori 《黑龙江环境通报》1988,8(4):281-286
Cytogenetic study of chorionic villi sampled because of advanced maternal age revealed, after overnight culture, an apparently non-mosaic trisomy 7. Amniocentesis showed exclusively normal mitoses, and the pregnancy continued normally. One hundred mitoses from cord blood of the normal newborn revealed a non-mosaic 46,XX complement. No cells with a proven trisomy 7 were found in cultures from either of two biopsies of the morphologically normal placenta, but the peripheral biopsy showed in multiple cultures an abnormal clone: 47,XX, + 20,-2,-21, + t(2;21)(p13;q22). To our knowledge, this is the first case of non-mosaic trisomy 7 detected on CVS which has had follow-up studies of amniotic fluid, cord blood, and term placenta. 相似文献
282.
283.
M. L. Smith O. L. Pellett M. M. J. Cass N. G. Kennaway N. R. M. Buist J. Buckmaster M. Golbus G. S. Spear J. A. Schneider 《黑龙江环境通报》1987,7(1):23-26
The prenatal diagnosis of cystinosis is currently based on the increased amount of free-cystine present in amniotic fluid cells. Amniocyte cultures must be grown for at least 2 weeks to obtain sufficient cells for such measurements. Thus, the diagnosis cannot be made until close to 20 weeks gestational age by this method. We report a case in which chorionic villi were used for direct cystine measurement resulting in the in utero diagnosis of cystinosis at 9 weeks gestational age. The diagnosis was confirmed by the study of cultured chorionic villus cells, and of the 10-week abortus. 相似文献
284.
The prenatal diagnosis of The Turner Syndrome is described at a menstrual age of 12 weeks. Detection of cystic hygroma was followed by vaginal chorionic villous sampling (CVS) which revealed a 45,X karyotype. Early documentation of fetal karyotype in the presence of a cystic hygroma is essential for accurate diagnosis and genetic counselling. 相似文献
285.
286.
Ants have a well developed olfactory sense, which they need both for the perception of environmental chemicals, and for a
highly sophisticated intraspecific communication system based on pheromones. The question arises therefore as to how different
odors are coded in the antennal lobe, the first central neuropil to process olfactory information. We measured odor-evoked
activity patterns using in vivo neuropil calcium recording in the antennal lobe of the ant Camponotus rufipes. We found that (a) odors elicit focal activity spots (diameter ca. 20 μm) which most probably represent the olfactory glomeruli;
(b) different odors are coded in odor specific patterns of such activated spots, and a particular spot can participate in
the pattern for different odors; (c) calcium increased in the activated spots within the 2-s stimulation period and slowly
declined thereafter.
Received: 10 March 1999 / Accepted in revised form: 5 July 1999 相似文献
287.
288.
289.
Sylvie Gagnon William Fraser Dr Bertrand Fouquette Adrien Bastide Marc Bureau Jean-Yves Fontaine Céline Huot 《黑龙江环境通报》1992,12(1):9-18
During a 7-year period, 117 fetal karyotypes were available from 131 genetic amniocenteses. These procedures were performed between 14 and 37 weeks' gestation for the following abnormal ultrasound findings: (1) intrauterine growth retardation (IUGR)—61 cases; (2) fetal malformation—71 cases; and (3) amniotic fluid volume (AFV) abnormality—60 cases. Chromosomal abnormalities were identified in 19 cases (16.2 per cent). Aneuploidy was 2.5 times as frequent in the presence of malformations than in their absence. No correlation was demonstrated between specific fetal malformations and specific chromosomal abnormalities. Aneuploidy was also twice as frequent in the presence of symmetrical IUGR than in its absence. No chromosomal abnormalities were found among eight cases of asymmetrical IUGR. Four cases of aneuploidy presented with isolated IUGR, three of these involving the X chromosome. The frequency of aneuploidy was the same with or without abnormalities of AFV (14.3 versus 16.4 per cent). No chromosomal abnormality was found associated with isolated AFV abnormalities. 相似文献
290.
M. Blunck W. -D. Busse G. Meister E. Möller A. Mullen L. A. A. van Rooijen 《Die Naturwissenschaften》1989,76(3):96-98
Online searching in publically available patent files opens up interesting possibilities to provide a rapid response to critical questions. A computerized analysis of all patents of leading German pharmaceutical companies over the last decade in important indication areas is described. Supported by subsequent manual processing of individual patents it is shown that duplicate experiments on animals practically never occur. 相似文献