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European Journal of Human Genetics : EJHG|June 23, 2011
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flowMalgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, 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.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 19, 2002
VASA is a specific marker for both normal and malignant human germ cellsAnne-Marie Zeeman, Hans Stoop, 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.
Reproductive Biomedicine Online|August 13, 2022
Chromosomal mosaicism in human blastocysts: a cytogenetic comparison of trophectoderm and inner cell mass after next-generation sequencingEffrosyni Chavli, Myrthe van den Born, Cindy Eleveld, 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.
Human Mutation|December 16, 2014
Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidiesDiane Van Opstal, Femke de Vries, Lutgarde Govaerts, et al.
Clinical Endocrinology|June 6, 2007
Impact of the Y-containing cell line on histological differentiation patterns in dysgenetic gonadsMartine Cools, Marjan Boter, Ruud van Gurp, et al.
European Journal of Human Genetics : EJHG|September 11, 2008
Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samplesDiane Van Opstal, Marjan Boter, Danielle de Jong, et al.
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