| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/PD.4967 |
| P698 | PubMed publication ID | 27862087 |
| P2093 | author name string | Joris Robert Vermeesch | |
| Mark I Evans | |||
| P2860 | cites work | Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification | Q24530153 |
| Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
| Pre-implantation genetic testing in ART: who will benefit and what is the evidence? | Q28072316 | ||
| Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis | Q28072788 | ||
| Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma | Q28314918 | ||
| High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays | Q29615979 | ||
| Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study. | Q30704921 | ||
| Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities | Q33905292 | ||
| Clinical diagnosis by whole-genome sequencing of a prenatal sample | Q34315784 | ||
| Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies | Q34484712 | ||
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| Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis | Q35552815 | ||
| Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies | Q36379133 | ||
| Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports | Q36402087 | ||
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| Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
| Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges | Q38188782 | ||
| Screening and Testing in Multiples | Q38847004 | ||
| Non-invasive detection of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advanced stage Hodgkin's lymphoma by sequencing of circulating cell-free DNA: a technical proof-of-principle study | Q38929950 | ||
| Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH). | Q40448517 | ||
| Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor | Q47810441 | ||
| Comparative analysis of comparative genomic hybridization microarray technologies: report of a workshop sponsored by the Wellcome Trust. | Q52599576 | ||
| Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus | Q56937251 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Rapid molecular method for prenatal detection of Down's syndrome | Q57436666 | ||
| Prenatal exclusion of β thalassaemia major by examination of maternal plasma | Q58029823 | ||
| P433 | issue | 13 | |
| P304 | page(s) | 1172-1177 | |
| P577 | publication date | 2016-12-06 | |
| P1433 | published in | Prenatal Diagnosis | Q15760059 |
| P1476 | title | Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening. | |
| P478 | volume | 36 |
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