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Expert Review of Molecular Diagnostics|February 12, 2016
Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberrationDiane Van Opstal, Malgorzata I SrebniakHuman Mutation|May 16, 2013
0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practiceMalgorzata I Srebniak, Lisanne Mout, Diane Van Opstal, et al.The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
The usefulness of calyculin a for cytogenetic prenatal diagnosisMalgorzata I Srebniak, Gizela G Trapp, Angelika K Wawrzkiewicz, et al.Best Practice & Research. Clinical Obstetrics & Gynaecology|September 7, 2024
Implementing non-invasive prenatal testing in a national screening program: Lessons learned from the TRIDENT studiesMatea Skojo, Malgorzata I Srebniak, Lidewij Henneman, et al.The Application of Clinical Genetics|May 22, 2023
Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome SequencingKarin E M Diderich, Jasmijn E Klapwijk, Vyne van der Schoot, et al.Prenatal Diagnosis|October 10, 2024
Confined Placental Mosaicism Detected With Non-Invasive Prenatal Testing: Is There an Association Between Mosaic Ratio and Pregnancy Outcome?Geerke M Eggenhuizen, Attie T J I Go, Mariëtte J V Hoffer, et al.American Journal of Medical Genetics. Part A|August 7, 2013
Deletion of 14.7 Mb 2q32.3q33.3 with a marfanoid phenotype and hypothyroidismAgnieszka Tomaszewska, Agnieszka Podbiol-Palenta, Marjan Boter, et al.Molecular Cytogenetics|December 6, 2011
Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effectMalgorzata I Srebniak, Marjan Boter, Carla Ma Verboven-Peerden, et al.Journal of Inherited Metabolic Disease|May 28, 2011
Prenatal screening of sialic acid storage disease and confirmation in cultured fibroblasts by LC-MS/MSJeroen van den Bosch, Linda F Oemardien, Malgorzata I Srebniak, et al.American Journal of Medical Genetics. Part A|January 21, 2016
The first de novo non-mosaic 14q11.2q13.1 tetrasomy of paternal originAgnieszka Tomaszewska, Jakub Behrendt, Marjan Boter, et al.Pageof 5