المؤلفون: Laura Bourlard, Yannick Manigart, Catherine Donner, Guillaume Smits, Julie Désir, Isabelle Migeotte, Bruno Pichon

المصدر: Journal of Perinatal Medicine. 50:476-485

مصطلحات موضوعية: HLA-G Antigens, Male, Pregnancy, Cell Line, Tumor, Noninvasive Prenatal Testing, Prenatal Diagnosis, Pediatrics, Perinatology and Child Health, Humans, Obstetrics and Gynecology, Female, Trophoblasts

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ded1973358cacbfe2f2341b8cd8c86Test
https://doi.org/10.1515/jpm-2021-0291Test

المؤلفون: Leonor Palmeira, Lore Lannoo, Anne De Leener, Eva Sammels, Julie Désir, Nathalie Brison, Guillaume Smits, Vincent Bours, Annelies Dheedene, Annelies Fieuw, Kris Van Den Bogaert, Marjan De Rademaeker, Elise Vantroys, Jean-Stéphane Gatot, Laura Bourlard, Vincent Gatinois, Colombine Meunier, Koenraad Devriendt, Armelle Duquenne, François Boemer, Bettina Blaumeiser, Axel Marichal, Katrien Janssens, Joris Vermeesch, Nathalie Fieremans, Bruno Pichon, Yves Sznajer, Björn Menten, Sandra Janssens, Bernard Grisart, Machteld Baetens, Damien Lederer

المساهمون: UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Centre de génétique médicale UCL

المصدر: Genetics in medicine
Genetics in medicine, Vol. 23, no.6, p. 1137-1142 (2021)

مصطلحات موضوعية: 0301 basic medicine, Down syndrome, medicine.medical_specialty, Noninvasive Prenatal Testing, Population, MEDLINE, Chromosome Disorders, Trisomy, Prenatal care, 030105 genetics & heredity, 03 medical and health sciences, Pregnancy, Prenatal Diagnosis, medicine, Humans, Genomic medicine, education, Genetics (clinical), education.field_of_study, business.industry, Obstetrics, Incidence (epidemiology), Aneuploidy, medicine.disease, 030104 developmental biology, Prenatal screening, Female, Human medicine, Down Syndrome, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4160c358ba3304c89c54ddec000e7f8Test
https://doi.org/10.1038/s41436-021-01101-4Test

المؤلفون: Bernard Grisart, Armelle Duquenne, Naïri Khudashvili, Margot van Riel, Eva Sammels, Leonor Palmeira, Elise Vantroys, Leen Vancoillie, Bruno Pichon, Nathalie Brison, Annelies Dheedene, Bettina Blaumeiser, Kris Van Den Bogaert, Katrien Janssens, Sandra Janssens, Axel Marichal, François Boemer, Machteld Baetens, Joris Vermeesch, Ilse Parijs, Yves Sznajer, Jean-Stéphane Gatot, Koenraad Devriendt, Annelies Fieuw, Laura Bourlard, Nathalie Fieremans, Julie Désir, Guillaume Smits, Saskia Bulk, Ellen Roets, Colombine Meunier, Marion Suenaert, Lore Lannoo, Anne De Leener, Lotte Vandeputte

المساهمون: UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Centre de génétique médicale UCL, UCL - (SLuc) Centre de référence neuromusculaire, UCL - (SLuc) Centre des maladies neuro-cutanées congénitales

المصدر: Obstetrics and gynecology
Obstetrics and gynecology, Vol. 137, no. 6, p. 1102-1108 (2021)

مصطلحات موضوعية: medicine.medical_specialty, Trisomy 13 Syndrome, Noninvasive Prenatal Testing, Aneuploidy, Trisomy, Sensitivity and Specificity, Multiple Gestation, Pregnancy, Quadruplet, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, medicine, Humans, Amnion, 030212 general & internal medicine, Diagnostic Errors, False Negative Reactions, Twin Pregnancy, Retrospective Studies, 030219 obstetrics & reproductive medicine, medicine.diagnostic_test, Genome, Human, Obstetrics, business.industry, Obstetrics and Gynecology, Retrospective cohort study, Chorion, Fetal Resorption, Pregnancy, Triplet, medicine.disease, Cohort, Amniocentesis, Pregnancy, Twin, Gestation, Female, Human medicine, Down Syndrome, Pregnancy, Multiple, business, Cell-Free Nucleic Acids, Trisomy 18 Syndrome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b528dfdf7f380424bf87e194c5212cbTest
https://hdl.handle.net/10067/1841600151162165141Test

المؤلفون: Sandra Janssens, Koenraad Devriendt, Joris Vermeesch, Julie Désir, J. Muys, Erik Fransen, Marjan De Rademaeker, Bettina Blaumeiser, Saskia Bulk, Katrien Janssens, Damien Lederer, Armelle Duquenne, Laura Bourlard, Björn Menten, Kathelijn Keymolen, Mauricette Jamar, Nathalie Brison, Ann Van Den Bogaert, Annelies Dheedene, Yves Sznajer, Yves Jacquemyn, Jean-Stéphane Gatot, Anne Destree, Bruno Pichon, Patrizia Chiarappa, Jorien Kerstjens, Annelies Fieuw, Kris Van Den Bogaert, Anne De Leener, Sonia Rombout

المساهمون: Clinical sciences, Medical Genetics

المصدر: Prenatal diagnosis

مصطلحات موضوعية: Male, 0301 basic medicine, Pediatrics, medicine.medical_specialty, DNA Copy Number Variations, Context (language use), 030105 genetics & heredity, Congenital Abnormalities, National cohort, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Belgium, Pregnancy, Prenatal Diagnosis, medicine, Humans, Copy-number variation, Genetics (clinical), Chromosome Aberrations, 030219 obstetrics & reproductive medicine, business.industry, Significant difference, Infant, Newborn, Pregnancy Outcome, Follow up studies, Infant, Obstetrics and Gynecology, Microarray Analysis, medicine.disease, Child development, eye diseases, Patient population, Case-Control Studies, Child, Preschool, Female, Human medicine, business, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b52db2e8dae2d0cf945fa66c52a30acTest
https://repository.uantwerpen.be/docstore/d:irua:2802Test