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Genes & Development|June 7, 2005
Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formationFemke A T de Vries, Esther de Boer, Mike van den Bosch, et al.Prenatal Diagnosis|September 19, 2017
Advanced genomic testing may aid in counseling of isolated agenesis of the corpus callosum on prenatal ultrasoundM C de Wit, F Boekhorst, G M Mancini, et al.Journal of Clinical Medicine|August 4, 2015
The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal TestingSam Riedijk, Karin E M Diderich, Sanne L van der Steen, et al.DNA Repair|July 13, 2005
Inactivation of RAD52 aggravates RAD54 defects in mice but not in Schizosaccharomyces pombeFemke A T de Vries, José B M Zonneveld, Annemarie van Duijn-Goedhart, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 23, 2016
Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeksM C de Wit, M I Srebniak, M Joosten, et al.Human Mutation|April 15, 2017
The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomaliesMalgorzata I Srebniak, Maarten F C M Knapen, Marike Polak, et al.The Journal of Experimental Medicine|June 22, 2016
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndromeMarije E C Meuwissen, Rachel Schot, Sofija Buta, et al.Pageof 2