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5 Rapid Prenatal Diagnosis of Chromosome Aneuploidies in Uncultured Amniocytes by Fluorescence in Situ Hybridization (Fish). Experience with 5,000 Patients


Book ID
121776304
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
194 KB
Volume
168
Category
Article
ISSN
1097-6868

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πŸ“œ SIMILAR VOLUMES


Two years' prospective experience using
✍ A. Morris; E. Boyd; S. Dhanjal; G. W. Lowther; D. A. Aitken; J. Young; A. L. Men πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 176 KB πŸ‘ 2 views

A probe was generated from the YAC clone 831B9 that was suitable for the prenatal detection of trisomy 21using fluorescence in situ hybridization (FISH). This probe was initially tested on a series of 650 unselected amniotic fluid samples prior to the karyotype being available. 630 were correctly id

PRENATAL DETECTION OF CHROMOSOME ANEUPLO
✍ THUE BRYNDORF; BRITTA CHRISTENSEN; MARIANNE VAD; JAN PARNER; VIBEKE BROCKS; JOHN πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 185 KB πŸ‘ 2 views

Successful rapid prenatal detection of selected numerical chromosome abnormalities by using fluorescence in situ hybridization (FISH) on uncultured amniotic fluid samples has been described by Klinger et al. (1992) and Ward et al. (1993Ward et al. ( , 1997)). Using essentially the same FISH protocol

Rapid positive confirmation of mosaicism
Systematic screening at diagnosis of βˆ’5/