Page 177 - FINAL PROGRAM

P-628 An ESHRE PGD Consortium multicentre retrospective cohort study investigating the clinical utility of PGD with human leukocyte antigen (HLA)-matching and factors in uencing a positive outcome
J. Traeger-Synodinos (Greece)
P-629 AMH and AMHR2 genes sequence variations in poor responders patients and controls – a pilot study
A. Leitao Marques (Portugal)
P-630 Validation of the de-novo segmental (> 16 megabase) loss detected by next generation sequencing in 24 blastocysts from preimplantation genetics diagnosis
Z. Shuang (China)
P-631 The proportion of aneuploidies is associated with the clinical outcome in patients with repetitive implantation failure undergoing pre-implantation genetic screening by aCGH C. Tabanelli (Italy)
P-632 A novel preimplantation genetic diagnosis strategy for Duchenne Muscular Dystrophy based on targeted Next-generation sequencing and linkage analysis
J. Du (China)
P-633 Next Generation Sequencing (NGS) metrics following DOP-PCR whole genome ampli cation (WGA) of single and multi-cell samples for PGS
M. Jasper (Australia)
P-634 Development of a universal method for the preimplantation diagnosis of β-thalassemia and sickle-cell anaemia using a novel next-generation sequencing approach: a new paradigm for PGD
D. Wells (United Kingdom)
P-635 Clinical outcome of SET transfer of euploid embryos by Next Generation Sequencing with and without MitoGrade(mitochondrial DNA selection)
K. Ravichandran (U.S.A.)
P-636 XRCC1 polymorphism Arg399Gln is associated with male infertility
A. Garcia (Spain)
P-637 Clinical application of sequencing-based Preimplantation Genetic Diagnosis
F. Chen (China)
P-638 Relationship between mitochondrial DNA quantity assessed by next generation sequencing (NGS) in blastocyst stage embryos and their implantation
S. Pukszta (Poland)
P-639 Identifying housekeeping genes that are stably expressed in the endometrium of both fertile women and those with recurrent implantation failure and recurrent miscarriages
L. Stocker (United Kingdom)
P-640 A powerful tagging Single Nucleotide Polymorphism method in terms of Next-Generation Sequencing that combines Preimplantation Genetic Diagnosis, informativity testing and aneuploidy screening
A.V. Penacho Martín (Spain)
FINAL PROGRAMME I HELSINKI, FINLAND – 3 TO 6 JULY 2016 173
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