| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/978-1-60761-947-5_11 |
| P953 | full work available at URL | https://link.springer.com/content/pdf/10.1007/978-1-60761-947-5_11 |
| P698 | PubMed publication ID | 20938838 |
| P2093 | author name string | Cathy Meaney | |
| Gail Norbury | |||
| P2860 | cites work | 'Touchdown' PCR to circumvent spurious priming during gene amplification | Q24630793 |
| Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma | Q28314918 | ||
| Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
| Rapid clearance of fetal DNA from maternal plasma | Q34388637 | ||
| Digital PCR: a powerful new tool for noninvasive prenatal diagnosis? | Q34878255 | ||
| MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. | Q36986986 | ||
| Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service | Q40626763 | ||
| Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma | Q47391690 | ||
| Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case report | Q47399906 | ||
| Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms | Q47423342 | ||
| Size distributions of maternal and fetal DNA in maternal plasma. | Q47432593 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Prenatal exclusion of β thalassaemia major by examination of maternal plasma | Q58029823 | ||
| Improvement in sensitivity of allele-specific PCR facilitates reliable noninvasive prenatal detection of cystic fibrosis | Q75424535 | ||
| Detection of fetal RHD-specific sequences in maternal plasma | Q77429872 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 155-172 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | Methods in Molecular Biology | Q15752859 |
| P1476 | title | Non-invasive prenatal diagnosis | |
| Non-invasive Prenatal Diagnosis | |||
| P478 | volume | 688 |
| Q33579048 | Experts' Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency - Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015). | cites work | P2860 |
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