Use of Fluorescent in Situ Hybridization to Detect Trisomy 13 in Archival Tissues for Cytogenetic Diagnosis
- 1 January 1992
- journal article
- Published by Taylor & Francis in Pediatric Pathology
- Vol. 12 (6) , 799-805
- https://doi.org/10.3109/15513819209024236
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Interphase cytogenetics in paraffin sections of routinely processed hydatidiform moles and hydropic abortionsThe Journal of Pathology, 1991
- Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectivelyClinical Genetics, 1991
- Use of in Situ Hybridization in Clinical CytogeneticsPediatric Pathology, 1991
- Interphase cytogeneticsNeurochemical Research, 1990