Final programme - eshre 2013

P-435 Triple-factor PGD for beta-thalassaemia, sideroblastic anaemia, combined with HLA-typing, employingthree different molecular approaches in a single blastomere: real-time nested-PCR, high-resolutionmelting (HRM) and fragment analysisG. Kakourou, M. Poulou, C. Vrettou, A. Destouni, J. Traeger-Synodinos, E. Kanavakis (Greece)P-436 multiple mutations discovered in a familial case of azoospermia using whole exome sequencing (WES)A.N. Yatsenko, A.P. Georgiadis, M.M. McGuire, M. Zorrilla, K.D. Bunce, D. Peters, A. Rajkovic,M. Olszewska, M. Kurpisz (U.S.A.)P-437 Clinical outcome assessment from pre-implantation genetic screening using array comparativegenomic hybridisation of polar bodies and blastomeres for embryo transfer selectionA.Z.A. Gilbertson, C.S. Ottolini, M.C. Summers, K. Sage, A.H. Handyside, A.R. Thornhill,D.K. Griffin (United Kingdom)P-438 positive clinical outcome after preimplantation genetic screening (PGS) using newly developed wholegenome array CGH platform after trophectoderm biopsyM.K. Chung, J.W. Kim, J.H. Lee, H.J. Jeong, M.H. Kim, M.J. Ryu, S.J. Park, H.Y. Kang, H.S. Lee (Korea South)P-439 Highly multiplexed targeted single-nucleotide polymorphism (SNP) amplification and sequencing as amethod for identifying fetal chromosomal disorders from maternal cell-free DNAB. Zimmermann, M. Banjevic, M. Hill, P. Lacroute, M. Dodd, S. Sigurjonsson, P. Lau, D. Prosen, N. Chopra,A. Ryan, M. Hall, S. McAdoo, Z. Demko, B. Levy, M. Rabinowitz (U.S.A.)P-440 introducing preimplantation genetic screening by array comparative genome hybridization in hungary:improving outcome of in vitro fertilizationA. Vereczeky, Z.S. Kósa, S. Sávay, M. Csenki, L. Nánássy, B. Dudás, Z.S. Dömötör, D. Debreceni (Hungary)P-441 frequency and characterization of blastocyst aneuplodyies after CGH-array analysis and its relationwith maternal ageA. Rossi, J.R. Alegretti, J. Cuzzi, M. Bonavita, M. Tanada, P. Matunaga, P. Fettback, M.B. Rosa, V. Maia,P. Hassun, E.L.A. Motta (Brazil)P-442 is morphological development of blastocysts correlated to chromosomal analysis by cgh-array aftertrophectoderm biopsy?M. Piccolomini, C. Gomes, B. Barros, M. Nicoliello, P. Matunaga, T. Criscuolo, M. Bonavita, J.R. Alegretti,E. Miyadahira, J. Cuzzi, P. Hassun, E.L.A. Motta (Brazil)P-443 dna methylation, genetic variants and ART outcome in oligozoospermiaD. Montjean, M. Benkhalifa, I. Berthaut, J.F. Griveau, K. Morcel, A. Bashamboo, K. McElreavey,C. Ravel (France)P-444 array-CGH versus FISH for PGS in recurrent miscarriage couplesC. Rubio, L. Rodrigo, E. Mateu, A. Mercader, V. Peinado, P. Buendia, M. Milán, A. Delgado, N. Al-Asmar,L. Escrich, I. Campos-Galindo, S. Garcia-Herrero, M.E. Poo, P. Mir, C. Simón (Spain)POSTERSP-445 single nucleotide polymorphisms (SNPs) related to neurotransmission associated with sperm qualityin infertile menA. Reyes-Engel, M. Cortes-Rodriguez, A. Lendinez, B. Perez-Nevot, A.R. Palomares, M. Ruiz Galdon (Spain)Programme book171