Zobrazeno 1 - 10
of 101
pro vyhledávání: '"W. Hammans"'
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 205:94-98
BACKGROUND In the past a non invasive risk analysis for detecting specific chromosomal aberrations was only possible from week 15 of pregnancy. In this paper the practicability of first trimester screening is analysed. MATERIAL AND METHODS Blood samp
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 125:1173-1177
Autor:
B. Eiben, W. Hammans
Publikováno v:
Reproduktionsmedizin. 15:372-377
Die Fluoreszenz-in-situ-Hybridisierung (FISH) an unkultivierten Fruchtwasserzellen hat sich in der vorgeburtlichen Diagnostik als Routineverfahren erfolgreich etabliert. Hierdurch konnen innerhalb von 24 h die haufigsten Chromosomenstorungen analysie
Publikováno v:
Fetal Diagnosis and Therapy. 14:193-197
Objective: A new method in prenatal diagnostics allows to demonstrate certain numeric chromosomal aneuploidies in amniotic cells within 24 h in contrast to conventional methods which take 1–3 weeks. Materials: The experience with this rapid fluores
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 123:55-57
Publikováno v:
Prenatal Diagnosis. 18:901-906
Fluorescence in situ hybridization (FISH) on uncultured amniocytes and standard cytogenetic analysis after amniocentesis have been performed for 904 samples. The experience with the FISH method and its clinical relevance is described in a large clini
Publikováno v:
Prenatal Diagnosis. 14:497-501
We report our cytogenetic experience of 1554 early amniocenteses between weeks 11 and 14 of gestation, of which 44 per cent were performed prior to week 14. The mean culture time was 14.5 days. Karyotyping was successful in 99.7 per cent of cases. In
Publikováno v:
Geburtshilfe und Frauenheilkunde. 53:554-558
Information is presented on 1100 early amniocenteses between the 12th and 14th week of gestation, performed at the Evangelisches Krankenhaus Oberhausen over a two year period. In all cases, a sufficient amount of amniotic fluid was obtained. In 99.7%
Autor:
M. Vogel, W. Hammans, Gesa Schwanitz, H. Hauss, S. Hansen, G. Stoltenberg, Bernd Eiben, R. Goebel, U. Gamerdinger, G. Rutt, M. Unger, A. Meyer
Publikováno v:
Prenatal Diagnosis. 12:945-950
The case of monosomy 18/ring chromosome 18 mosaicism which was detected prenatally by amniocentesis is presented. The pregnancy was terminated in week 18. Autopsy showed complex malformation of the fetus consisting of cebocephaly, hypotelorism, micro
Publikováno v:
Prenatal Diagnosis. 18:87-89