Page 301 - PROGRAMME2018

P-608 Level of embryonic mosaicism do not seem to be influenced by extrinsic features: analysis of 298 mosaic embryos
M.G. Minasi1, F. Fiorentino2, A. Ruberti1, A. Biricik2, E. Cursio1, S. Bono2, A. Colasante1, E. Cotroneo2, V. Casciani1, F. Scarselli1, R. Polese1, M.T. Varricchio1, M. Baldi2, F. Spinella2, E. Greco1
1European Hospital, Center for Reproductive Medicine, Rome, Italy 2GENOMA Group, Molecular Genetics Laboratories, Rome, Italy
P-609 Cryptic complexity identified by whole-genome mate-pair sequencing in complex chromosomal rearrangements: implications on preimplantation genetic diagnosis and reproductive genetic counseling
C. Aristidou1, E. Constantinou1, A. Alexandrou1, A. Theodosiou1, M. Mehrjouy2, M. Bak2, N. Tommerup2, C. Sismani1
1The Cyprus Institute of Neurology and Genetics, Department of Cytogenetics and Genomics, Nicosia, Cyprus
2University of Copenhagen, Wilhelm Johannsen Centre for Functional Genome Research- Department of Cellular and Molecular Medicine, Copenhagen, Denmark
P-610 Introducing direct CGG repeat analysis in preimplantation genetic diagnosis (PGD) for fragile X syndrome: an overview of clinical outcomes for 116 patients
R. Cabey1, D. Nusblat1, J. Gay1, E. Armenti1, B. Chu2, N. Goodall2, R. Prates2, M. Konstantinidis2 1CooperGenomics, genetic counseling, Livingston- New Jersey, U.S.A.
2CooperGenomics, laboratory, Livingston- New Jersey, U.S.A.
P-611 External verification of the Agilent Technologies OnePGT solution for PGT-M on blastomere and trophectoderm biopsies from UZ Leuven
C. Melotte1, E. Dimitriadou1, M. Zamani Esteki2, H. Masset3, K.O. François4, J. Allemeersch4, R. Richards4, S. Moeys4, J. Theuns4, J.R. Vermeesch1
1Leuven University Hospital, Center for Human Genetics, Leuven, Belgium
2Center for Human Genetics- KU Leuven, Laboratory of Reproductive Genomics, Leuven, Belgium
3Center for Human Genetics- KU Leuven, Laboratory for Cytogenetics and Genome Research, Leuven, Belgium
4Agilent Technologies, Agilent Technologies, Leuven, Belgium
P-612 A proposed method to minimize male gamete contribution to aneuploidy in the embryo cohort
A. Melnick1, A. Parrella1, S. Cheung1, P. Xie1, Z. Rosenwaks1, G. Palermo1
1Weill Cornell Medicine, The Ronald O. Perelman and Claudia Cohen Center for Reproductive Medicine, New York, U.S.A.
P-613 Genomic profiling of spermatogenetic function in azoospermic men
B. Chin1, S. Cheung1, C. O'Neill1, Z. Rosenwaks1, G. Palermo1
1Weill Cornell Medicine, The Ronald O. Perelman and Claudia Cohen Center for Reproductive Medicine, New York, U.S.A.
FINAL PROGRAMME I BARCELONA, SPAIN – 1 TO 4 JULY 2018 301
POSTERS