| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1537-2995.2012.03738.X |
| P698 | PubMed publication ID | 22691192 |
| P50 | author | Thomas Müller | Q63788179 |
| P2093 | author name string | Franz F Wagner | |
| Andrea Doescher | |||
| Eduard K Petershofen | |||
| Markus Schunter | |||
| P2860 | cites work | Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience | Q34192088 |
| A multiplex assay with 52 single nucleotide polymorphisms for human identification | Q34508959 | ||
| Non-invasive antenatal RHD typing | Q36431820 | ||
| Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study | Q36538133 | ||
| Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects | Q37351817 | ||
| Report of the first nationally implemented clinical routine screening for fetal RHD in D- pregnant women to ascertain the requirement for antenatal RhD prophylaxis | Q46172895 | ||
| Size distributions of maternal and fetal DNA in maternal plasma. | Q47432593 | ||
| Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing. | Q53288194 | ||
| The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible. | Q54520641 | ||
| Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. | Q54574187 | ||
| Noninvasive determination of fetal RHD status by examination of cell-free DNA in maternal plasma. | Q54646324 | ||
| Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RhD-negative pregnancies. | Q54677055 | ||
| Fetal RhD genotyping by maternal serum analysis: a two-year experience. | Q54677407 | ||
| Prenatal genotyping of RHD and SRY using maternal blood. | Q54741354 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| P433 | issue | 2 | |
| P921 | main subject | single-nucleotide polymorphism | Q501128 |
| P304 | page(s) | 353-362 | |
| P577 | publication date | 2012-06-13 | |
| P1433 | published in | Transfusion | Q15758500 |
| P1476 | title | Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups | |
| P478 | volume | 53 |
| Q36423067 | 14 Years of Polish Experience in Non-Invasive Prenatal Blood Group Diagnosis |
| Q102152274 | Detection of cell-free foetal DNA fraction in female-foetus bearing pregnancies using X-chromosomal insertion/deletion polymorphisms examined by digital droplet PCR |
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| Q98945760 | Introduction of Noninvasive Prenatal Testing for Blood Group and Platelet Antigens from Cell-Free Plasma DNA Using Digital PCR |
| Q48141047 | Molecular typing for blood group antigens within 40 min by direct polymerase chain reaction from plasma or serum |
| Q35507579 | Non-Invasive Prenatal RHD Genotyping Using Cell-Free Fetal DNA from Maternal Plasma: An Italian Experience |
| Q50631143 | Non-invasive prenatal diagnosis of monogenic disorders: an optimized protocol using MEMO qPCR with miniSTR as internal control. |
| Q87466211 | Noninvasive fetal RhD genotyping |
| Q35049156 | Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests |
| Q33416691 | Platelet recovery and survival measured in patients by quantitative polymerase chain reaction of mitochondrial DNA. |
| Q102331644 | Prenatal RHD genotyping in Croatia: preliminary results |
| Q36423155 | The Glass Slide Extraction System Snap Card Improves Non-Invasive Prenatal Genotyping in Pregnancies with Antibodies |
| Q48339604 | Vox Sanguinis International Forum on application of fetal blood grouping. |
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