Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
- 1 November 2006
- journal article
- research article
- Published by Elsevier in Genetics in Medicine
- Vol. 8 (11) , 719-727
- https://doi.org/10.1097/01.gim.0000245576.47154.63
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluidJournal of Human Genetics, 2006
- Single-cell chromosomal imbalances detection by array CGHNucleic Acids Research, 2006
- A high-resolution survey of deletion polymorphism in the human genomeNature Genetics, 2005
- Development and validation of a CGH microarray for clinical cytogenetic diagnosisGenetics in Medicine, 2005
- Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?American Journal of Medical Genetics Part A, 2005
- DNA identification of fetal cells isolated from cervical mucus: potential for early non‐invasive prenatal diagnosisBJOG: An International Journal of Obstetrics and Gynaecology, 2005
- Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second‐trimester amniocentesesPrenatal Diagnosis, 2004
- Microarray Analysis of Cell-Free Fetal DNA in Amniotic Fluid: a Prenatal Molecular KaryotypeAmerican Journal of Human Genetics, 2004
- Detection of large-scale variation in the human genomeNature Genetics, 2004
- Assessment of Demand for Prenatal Diagnostic Testing Using Willingness to PayObstetrics & Gynecology, 2004