Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays
- 1 November 2010
- journal article
- research article
- Published by Elsevier in Fertility and Sterility
- Vol. 94 (6), 2017-2021
- https://doi.org/10.1016/j.fertnstert.2010.01.052
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- A novel single-cell DNA fingerprinting method successfully distinguishes sibling human embryosFertility and Sterility, 2009
- Perspectives on the efficacy and indications for preimplantation genetic screening: where are we now?Human Reproduction, 2008
- Oocyte karyotyping by comparative genomic hybrydization provides a highly reliable method for selecting “competent” embryos, markedly improving in vitro fertilization outcome: a multiphase studyFertility and Sterility, 2007
- High resolution array-CGH analysis of single cellsNucleic Acids Research, 2006
- Single-cell chromosomal imbalances detection by array CGHNucleic Acids Research, 2006
- Aneuploidy detection in single cells using DNA array-based comparative genomic hybridizationMolecular Human Reproduction, 2004
- Positive outcome after preimplantation diagnosis of aneuploidy in human embryos *Human Reproduction, 1999
- Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisationNucleic Acids Research, 1999
- Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation.BMJ, 1993
- Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers.Proceedings of the National Academy of Sciences, 1989