| scholarly article | Q13442814 |
| P356 | DOI | 10.1196/ANNALS.1368.013 |
| P8608 | Fatcat ID | release_kmgup6c7rvbqna4xj6mxecgh4e |
| P698 | PubMed publication ID | 17108198 |
| P50 | author | Supan Fucharoen | Q88047307 |
| P2093 | author name string | Goonnapa Fucharoen | |
| Thawalwong Ratanasiri | |||
| Kanokwan Sanchaisuriya | |||
| Warunee Tungwiwat | |||
| P2860 | cites work | Prenatal sex determination by DNA amplification from maternal peripheral blood | Q34465871 |
| Maternal plasma fetal DNA as a marker for preterm labour. | Q50851221 | ||
| Non-invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma. | Q54764349 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Elevation of both maternal and fetal extracellular circulating deoxyribonucleic acid concentrations in the plasma of pregnant women with preeclampsia | Q57671390 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 103-107 | |
| P577 | publication date | 2006-09-01 | |
| P1433 | published in | Annals of the New York Academy of Sciences | Q2431664 |
| P1476 | title | Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma. | |
| P478 | volume | 1075 |
| Q28069689 | A Dormant Microbial Component in the Development of Preeclampsia |
| 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 |
| Q54522825 | Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion: application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalis. |
| Q81507580 | Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia |
| Q47159911 | Association of Tissue-Specific DNA Methylation Alterations with α-Thalassemia Southeast Asian Deletion |
| Q52883296 | COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma. |
| Q54941025 | Decreased DNA methylation of a CpG site in the HBAP1 gene in plasma DNA from pregnant women. |
| Q35544890 | Efficiency assessment of immunochromatographic strip test for the diagnosis of alpha-thalassemia-1 carriers |
| Q28388335 | Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases |
| Q38089080 | Molecular diagnostics for haemoglobinopathies |
| Q38002933 | Noninvasive prenatal diagnosis of monogenic disorders |
| Q55424946 | Prenatal detection of thalassemia by cell-free fetal DNA (cffDNA) in maternal plasma using surface enhanced Raman spectroscopy combined with PCR. |
| Q34042854 | Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma |
| Q38099617 | The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made |
| Q38048368 | Universal screening for inherited metabolic diseases in the neonate (and the fetus). |
Search more.