| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0140-6736(02)11086-5 |
| P698 | PubMed publication ID | 12383672 |
| P50 | author | Tze Kin Lau | Q51980546 |
| David H K Chui | Q66829380 | ||
| P2093 | author name string | Rossa W K Chiu | |
| Y M Dennis Lo | |||
| Katherine C K Chow | |||
| Tse N Leung | |||
| P2860 | cites work | Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma | Q28314918 |
| The thalassaemias | Q30499105 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screening | Q73254798 | ||
| New strategy for prenatal diagnosis of X-linked disorders | Q74053620 | ||
| P433 | issue | 9338 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 998-1000 | |
| P577 | publication date | 2002-09-01 | |
| P1433 | published in | The Lancet | Q939416 |
| P1476 | title | Prenatal exclusion of beta thalassaemia major by examination of maternal plasma | |
| P478 | volume | 360 |
| Q37155440 | 10. Circulating Nucleic Acids as Diagnostic Tool |
| Q40201029 | A Pilot Study of Noninvasive Prenatal Diagnosis of Alpha- and Beta-Thalassemia with Target Capture Sequencing of Cell-Free Fetal DNA in Maternal Blood |
| Q33221593 | Alpha-thalassaemia and population health in Southeast Asia. |
| Q90724412 | Analysis of fetal DNA in maternal plasma with markers designed for forensic DNA mixture resolution |
| Q38331030 | Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran |
| Q81507580 | Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia |
| Q37801660 | Application of proteomics to prenatal screening and diagnosis for aneuploidies. |
| Q35966472 | Cell-free fetal DNA in maternal blood: kinetics, source and structure |
| Q36733657 | Cell-free fetal DNA in maternal plasma and noninvasive prenatal diagnosis |
| Q28241617 | Cell-free fetal DNA in maternal plasma: an important advance to link fetal genetics to obstetric ultrasound |
| Q36152745 | Cell-free fetal DNA in the maternal circulation and its future uses in obstetrics |
| Q39778751 | Cell-free fetal nucleic acids as prenatal biomarkers |
| Q34426839 | Cell-free nucleic acids as non-invasive biomarkers of gynecological cancers, ovarian, endometrial and obstetric disorders and fetal aneuploidy |
| Q58035393 | Circulating nucleic acids as a new diagnostic tool |
| Q36790198 | Circulating nucleic acids in plasma and serum: applications in diagnostic techniques for noninvasive prenatal diagnosis |
| Q88990659 | Current approaches on non-invasive prenatal diagnosis: Prenatal genomics, transcriptomics, personalized fetal diagnosis |
| Q53674441 | Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening. |
| Q34078379 | Detection of the placental epigenetic signature of the maspin gene in maternal plasma. |
| Q54443778 | Development of a PCR/LDR/capillary electrophoresis assay with potential for the detection of a beta-thalassemia fetal mutation in maternal plasma. |
| Q34239768 | Differential DNA methylation as a tool for noninvasive prenatal diagnosis (NIPD) of X chromosome aneuploidies |
| Q34575372 | Differentially expressed microRNAs in maternal plasma for the noninvasive prenatal diagnosis of Down syndrome (trisomy 21). |
| Q35916813 | Digital PCR for the molecular detection of fetal chromosomal aneuploidy |
| Q34558118 | Epigenetic approaches for the detection of fetal DNA in maternal plasma |
| Q58106704 | Ethical Concerns in the Implementation of DNA Sequencing-Based Noninvasive Prenatal Testing for Fetal Aneuploidy Among Obstetric Professionals in Hong Kong |
| Q34425220 | Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis |
| Q36654711 | Fetal DNA in maternal plasma: progress through epigenetics |
| Q35990077 | Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin |
| Q59001540 | Fetal Nucleic Acids in Maternal Circulation: A Genetic Resource for Noninvasive Prenatal Diagnosis |
| Q26863327 | Free DNA--new potential analyte in clinical laboratory diagnostics? |
| Q33257556 | Genotyping fetal paternally inherited SNPs by MALDI-TOF MS using cell-free fetal DNA in maternal plasma: influence of size fractionation |
| Q45859656 | Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. |
| Q35611090 | Invasive & non-invasive approaches for prenatal diagnosis of haemoglobinopathies: experiences from India |
| Q38181003 | Lab-on-a-chip technology: impacting non-invasive prenatal diagnostics (NIPD) through miniaturisation |
| Q53863271 | LigAmp for sensitive detection of single-nucleotide differences. |
| Q33737845 | MALDI-TOF MS in Prenatal Genomics |
| Q33263722 | MALDI-TOF mass spectrometry for quantitative, specific, and sensitive analysis of DNA and RNA. |
| Q36986986 | MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. |
| Q36098624 | Medical genetics and genomic medicine in Greece: achievements and challenges. |
| Q58256594 | Microarray Detection of Fetal DNA Levels in Maternal Plasma |
| Q35784169 | Molecular diagnosis of haemoglobin disorders |
| Q36247154 | Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies |
| Q38089080 | Molecular diagnostics for haemoglobinopathies |
| Q37316945 | Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia. |
| Q35667087 | Non-Invasive Prenatal Diagnosis in the Management of Preimplantation Genetic Diagnosis Pregnancies |
| Q85181748 | Non-invasive Prenatal Diagnosis |
| Q34688588 | Non-invasive prenatal detection of achondroplasia using circulating fetal DNA in maternal plasma |
| Q37809306 | Non-invasive prenatal diagnosis by fetal nucleic acid analysis in maternal plasma: the coming of age |
| Q54313935 | Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis. |
| Q38770436 | Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis. |
| Q36117921 | Non-invasive prenatal diagnosis using cell-free fetal nucleic acids in maternal plasma: Progress overview beyond predictive and personalized diagnosis |
| Q35885009 | Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms |
| Q35073312 | Non-invasive prenatal diagnosis: on the horizon? |
| Q54184929 | Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing. |
| Q50051267 | Non-invasive prenatal testing for fetal inheritance of maternal β-thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study |
| Q37809342 | Noninvasive Approaches to Prenatal Diagnosis of Hemoglobinopathies Using Fetal DNA in Maternal Plasma |
| Q38549770 | Noninvasive Prenatal Screening for Genetic Diseases Using Massively Parallel Sequencing of Maternal Plasma DNA |
| Q26783426 | Noninvasive prenatal diagnosis |
| Q44912114 | Noninvasive prenatal diagnosis experience in the Çukurova Region of Southern Turkey: detecting paternal mutations of sickle cell anemia and β-thalassemia in cell-free fetal DNA using high-resolution melting analysis |
| Q37000915 | Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma |
| Q38002933 | Noninvasive prenatal diagnosis of monogenic disorders |
| Q37705437 | Noninvasive prenatal diagnosis using ccffDNA in maternal blood: state of the art. |
| Q37866719 | Novel approaches to manipulating foetal cells in the maternal circulation for non-invasive prenatal diagnosis of the unborn child |
| Q35839919 | Performance of Droplet Digital PCR in Non-Invasive Fetal RHD Genotyping - Comparison with a Routine Real-Time PCR Based Approach |
| Q34955670 | Placental mRNA in maternal plasma: prospects for fetal screening |
| Q38954748 | Prenatal and pre-implantation genetic diagnosis |
| Q73398751 | Prenatal detection of fetal hemoglobin E gene from maternal plasma |
| Q36673937 | Prenatal diagnosis: progress through plasma nucleic acids |
| Q37322448 | Prenatal diagnosis: update on invasive versus noninvasive fetal diagnostic testing from maternal blood |
| Q37181558 | Rapid and non invasive prenatal diagnosis. |
| Q36063025 | Recent advances in fetal nucleic acids in maternal plasma |
| Q37000825 | Recent advances in non-invasive prenatal DNA diagnosis through analysis of maternal blood. |
| Q33237610 | Recent developments in fetal nucleic acids in maternal plasma: implications to noninvasive prenatal fetal blood group genotyping |
| Q33274418 | Recent developments in the detection of fetal single gene differences in maternal plasma and the role of size fractionation |
| Q38594354 | Recent patents and technology transfer for molecular diagnosis of β-thalassemia and other hemoglobinopathies |
| Q34042854 | Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma |
| Q91936492 | Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases |
| Q38625435 | Thalassemia 2016: Modern medicine battles an ancient disease |
| Q30250029 | The accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis. |
| Q35879299 | The biology and diagnostic applications of fetal DNA and RNA in maternal plasma |
| Q38099617 | The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made |
| Q78840671 | The ins and outs of fetal DNA in maternal plasma |
| Q26995586 | Tracking fetal development through molecular analysis of maternal biofluids |
| Q34960254 | mRNA of placental origin is readily detectable in maternal plasma. |
Search more.