Application of fluorescentin situ hybridization for ‘de novo’ anomalies in prenatal diagnosis
- 1 September 1993
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 13 (9) , 825-832
- https://doi.org/10.1002/pd.1970130906
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Molecular cytogenetic and clinical studies of 42 patients with marker chromosomesAmerican Journal of Medical Genetics, 1992
- Maternal serum alpha‐fetoprotein levels and fetal outcome in early second‐trimester oligohydramniosPrenatal Diagnosis, 1992
- Chorionic villus metaphase chromosomes and interphase nuclei analysed by chromosomalin situ suppression (CISS) hybridizationPrenatal Diagnosis, 1992
- Construction and characterization of plasmid libraries enriched in sequences from single human chromosomesGenomics, 1991
- Chromosome in situ suppression hybridisation in clinical cytogenetics.Journal of Medical Genetics, 1991
- Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogeneticsHuman Genetics, 1990
- Isolation and characterization of an ?-satellite repeated sequence from human chromosome 22Chromosoma, 1986
- Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.Proceedings of the National Academy of Sciences, 1986
- Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21Cytogenetic and Genome Research, 1986
- Distal 15q trisomy with Dandy-Walker malformation in a female infantJournal of Human Genetics, 1985