Detalles de la búsqueda
1.
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.
Am J Hum Genet
; 109(6): 1140-1152, 2022 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35659929
2.
Detection of DNA Contamination in Prenatal Samples from Whole Exome Sequencing Data.
Clin Chem
; 2024 Jun 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-38863407
3.
All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.
Prenat Diagn
; 43(4): 527-543, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36647814
4.
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Am J Hum Genet
; 105(6): 1091-1101, 2019 12 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31708118
5.
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.
Am J Hum Genet
; 109(7): 1344, 2022 Jul 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35803237
6.
Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Genet Med
; 20(5): 480-485, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29121006
7.
Combined Count- and Size-Based Analysis of Maternal Plasma DNA for Noninvasive Prenatal Detection of Fetal Subchromosomal Aberrations Facilitates Elucidation of the Fetal and/or Maternal Origin of the Aberrations.
Clin Chem
; 63(2): 495-502, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27974386
8.
Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.
J Genet Couns
; 26(6): 1348-1356, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28667567
9.
Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations.
Prenat Diagn
; 36(3): 216-23, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26774010
10.
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.
Prenat Diagn
; 36(12): 1091-1098, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27739584
11.
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
Prenat Diagn
; 36(12): 1083-1090, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27750376
12.
Cell-Free RNA Is a Reliable Fetoplacental Marker in Noninvasive Fetal Sex Determination.
Clin Chem
; 61(12): 1515-23, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26467504
13.
Current controversies in prenatal diagnosis 1: NIPT for chromosome abnormalities should be offered to women with low a priori risk.
Prenat Diagn
; 35(1): 8-14, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25393690
14.
Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment.
Prenat Diagn
; 35(6): 549-57, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25644120
15.
Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testing.
EBioMedicine
; 100: 104983, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38365322
16.
Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies.
Prenat Diagn
; 33(6): 563-8, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23613171
17.
Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience.
Prenat Diagn
; 32(4): 362-70, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22467167
18.
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.
J Clin Oncol
; 40(22): 2426-2435, 2022 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35394817
19.
The 2014 Malcolm Ferguson-Smith Young Investigator Award.
Prenat Diagn
; 35(6): 515-6, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26041253
20.
In case you missed it: the Prenatal Diagnosis editors bring you the most significant advances of 2014.
Prenat Diagn
; 35(1): 29-34, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25594313