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991.
Während der Vorbereitungen zu diesem Artikel war R. L. J. als Preisträger der Alexander-von-Humboldt-Stiftung in Göttingen tätig. Unsere Forschung auf diesem Gebiet wurde durch großzügige Hilfe der Deutschen Forschungsgemeinschaft und der National Science Foundation (USA) ermöglicht. Außerdem sind wir B. Raufeisen für die Herstellung der Zeichnungen sehr zu Dank verpflichtet. 相似文献
992.
993.
J.C Jones 《Journal of Loss Prevention in the Process Industries》1998,11(6):407-411
A new criterion for shipping safety of activated carbons is developed which requires microcalorimetric measurements for its implementation. It is examined by making microcalorimetric measurements on a variety of commercial activated carbons. Results are compared with those for the same carbons according to the critical ignition temperature approach. 相似文献
994.
995.
Finn Stener Jørgensen MD Jens Bang Lisbeth Tranebjærg Lillian N. Berge Sturla H. Eik-Nes Marianne Schwartz 《黑龙江环境通报》1994,14(2):149-152
We present a case of prenatal diagnosis of cystic fibrosis (CF) in one twin at 11–12 weeks of gestation. The parents had previously had two children, one of whom is alive and healthy and one who died of CF at the age of 2½ months. The parents were both known to be carriers of the ΔF508 mutation. Chorionic villus sampling (CVS) was performed and direct gene analysis showed that one fetus was homozygous for the ΔF508 mutation, while the other fetus did not have the mutation at all. Both fetuses had normal karyotypes. Selective termination was subsequently performed. The pregnancy continued without complications except for mild pre-eclampsia at term. The woman had a Caesarean section. The genetic diagnosis was confirmed after birth. 相似文献
996.
We report the detection of a mosaic triple trisomy, 46, XY/49, XY, + 13, +20, +21, in two amniotic fluid specimens obtained from a pregnancy that yielded a normal infant. Traditional cytogenetic methods failed to detect the abnormal cell lineage in fetal blood, foreskin, amnion, umbilical cord, and three different biopsies of the chorion. In addition, fluorescence in situ hybridization study of cells from a buccal smear showed no evidence of cells with three copies of chromosome 20. 相似文献
997.
998.
Gastrointestinal tract atresia has an incidence of 1 in 10 000 live-births, while gastric outlet obstruction comprises only approximately 1 per cent of these malformations. A prenatally diagnosed case is described, followed by a discussion regarding the diagnosis and possible associated abnormalities. 相似文献
999.
1000.
Holoprosencephaly is a cerebral anomaly resulting from incomplete cleavage of the primitive prosencephalon or forebrain. Early detection of this anomaly is very important since the most severe form is incompatible with life. The diagnosis also signals the need for a chromosomal determination since chromosomal abnormalities have been associated with this anomaly. An early diagnosis of alobar holoprosencephaly at 14 weeks' gestation, employing transvaginal sonography, is reported. Our findings are compared with prenatal transabdominal sonographic findings of holoprosencephaly which have been reported during the last decade in the literature. 相似文献