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A metabolomics-based approach for non-invasive diagnosis of chromosomal anomaliesDOI 10.1007/s11306-017-1274-z
Prenatal Metabolomics Analysis and Fetal Congenital Anomalies and Genetic Conditions: A Review of Current LiteratureSemantic proximity
Metabolomic analysis for first-trimester Down syndrome predictionSemantic proximity
Untargeted metabolomics: an overview of its usefulness and future potential in prenatal diagnosisSemantic proximity
Potential role of “omics” technique in prenatal diagnosis of congenital heart defectsSemantic proximity
Metabolomic prediction of fetal congenital heart defect in the first trimesterSemantic proximity
Update on the use of exome sequencing in the diagnosis of fetal abnormalitiesSemantic proximity
Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalitiesSemantic proximity
The Multi-Omic Approach to Newborn Screening: Opportunities and ChallengesSemantic proximity
The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal AbnormalitiesSemantic proximity
Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal DiagnosisSemantic proximity
Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defectsSemantic proximity
Celomic Fluid: Laboratory Workflow for Prenatal Diagnosis of Monogenic DiseasesSemantic proximity
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