Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study
- 23 February 2000
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 20 (2) , 123-131
- https://doi.org/10.1002/(sici)1097-0223(200002)20:2<123::aid-pd762>3.0.co;2-b
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Identification and characterization of ade novopartial trisomy 10p by comparative genomic hybridization (CGH)Clinical Genetics, 1998
- A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.Journal of Medical Genetics, 1998
- Minimal sizes of deletions detected by comparative genomic hybridizationGenes, Chromosomes and Cancer, 1998
- Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotypeHuman Genetics, 1997
- Quantitative analysis of comparative genomic hybridizationCytometry, 1995
- Hardware and software requirements for quantitative analysis of comparative genomic hybridizationCytometry, 1995
- Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescencein situhybridizationPrenatal Diagnosis, 1994
- Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridizationHuman Genetics, 1993
- Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid TumorsScience, 1992
- Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84Human Genetics, 1986