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P-590 Chromosomal mosaicism in spontaneous abortions: a case-control molecular cytogenetics study of 1280 specimens by interphase FISH
S. Vorsanova1, O. Kurinnaia1, Y. Yurov2, A. Kolotii1, I. Demidova1, V. Kravets1, M. Zelenova2, K. Vasin2, M. Gordeeva1, S. Fedorenko2, I. Iourov2
1Academician Yu.E. Veltishchev Research Clinical Institute of Pediatrics- N.I. Pirogov Russian National Research Medical University- Ministry of Health of the Russian Federation- Moscow, Laboratory of molecular cytogenetics of neuropsychiatric diseases,
2FSBSI «Mental Health Research Center»- Moscow, Laboratory of cytogenetics, Moscow, Russia C.I.S.
P-591 Application of SMRT Sequencing in preimplantation genetic testing (PGT) for reciprocal translocation carriers
L. Hu1, J. Zhou2, D. Cheng3, K. Luo4, F. Gong4, Y. Tan4, P. Xie5, D. Wang2, G. Lu6, K. Wang7, G. Lin4
1Institute of Reproductive and Stem Cell Engineering- School of Basic Medical Science, Central South University, Changsha, China
2Nextomics Biosciences, Nextomics Biosciences, Wuhan, China
3Reproductive and Genetic Hospital of Citic-Xiangya, Genetic Center, Changsha, China
4School of Basic Medical Science- Central South University, Institute of Reproductive and Stem Cell Engineering, Changsha, China
5National Engineering and Research Center of Human Stem Cells, R&D department, Changsha, China
6National Engineering and Research Center of Human Stem Cells, National Engineering and Research Center of Human Stem Cells, Changsha, China
7Columbia University, Institute for Genomic Medicine, New York, U.S.A.
P-592 Comparison of euploid embryo formation after natural or mild stimulation
M. Terribile1, M. Wilding1, I. Parisi1, T. Pehlivan1, V. Hall1, G. Nargund1 1Create Fertility, Embryology, London, United Kingdom
P-594 Novel loss of function mutations of follicle-stimulating hormone receptor in a patient with premature ovarian insufficiency identified by infertility gene panel using next generation sequencing
S. Van Dooren1, A. Sassi2, J. Désir3, S. Costagliola4, V. Janssens5, M. Bonduelle6, A. Gheldof6, D. Daneels6, A. Delbaere2
1UZ Brussel, Centre for Medical Genetics & BRIGHTcore, Jette- Brussels, Belgium
2Erasme Hospital- Université Libre de Bruxelles, Fertility Clinic- Department of Obstetrics and Gynecology, Brussels, Belgium
3Erasme Hospital- Université Libre de Bruxelles- Brussels- Belgium, Department of Genetics, Brussels, Belgium
4Université Libre de Bruxelles, IRIBHM- Institute of Interdisciplinary Research in Human and Molecular Biology-, Brussels, Belgium
5Université Libre de Bruxelles -, IRIBHM- Institute of Interdisciplinary Research in Human and Molecular Biology, Brussels, Belgium
6UZ Brussel- Vrije Universiteit Brussel, Centre for Medical Genetics- Reproduction and Genetics- Reproduction and Genetics and Regenerative Medicine, Brussels, Belgium
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