Page 264 - Eshre Final Programme 2015

P-619 FISH is equivalent to SNP array for preimplantation genetic diagnosis on young translocation carriers undergoing blastocyst biopsy
C. Dehua1, L. Keli2, T. Ke3, G. Fei4, L. Changfu4, Z. Shuoping4, G. Yifan4, L. Guangxiu4, L. Ge4, T. Yueqiu5
1Institute of Reproductive & Stem Cell Engineering Central South University Changsha Hunan China.Reproductive & Genetic Hospital of CITIC-Xiangya Genetic Center Changsha Hunan China, Genetic Center, Changsha, China
2Reproductive and Genetic Hospital of Citic-Xiangya Changsha HunanP.R.China, Reproductive Center, Changsha, China
3Institute of Reproductive & Stem Cell Engineering Central South University Changsha Hunan China., Gentic Center, Changsha, China
4Institute of Reproductive & Stem Cell Engineering Central South University Changsha Hunan China., Reproductive Center, Changsha, China
5Institute of Reproductive & Stem Cell Engineering Central South University Changsha Hunan China.Reproductive & Genetic Hospital of CITIC-Xiangya Genetic Center Changsha Hunan China, Gentic Center, Changsha, China
P-620 The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridisation.
H. Ghevaria1, S. SenGupta1, P. Serhal2, J. Delhanty1
1University College London, Institute for Womens Health UCL Centre for PGD, London, United Kingdom
2The Centre for Reproductive and Genetic Health, The New Wing Eastman Dental Hospital, London, United Kingdom
P-621 Polymorphism of CAG and GGN Repeats in Androgen Receptor Gene in Women with Polycystic Ovary Syndrome
C. Yuan1, Y. Qian1, Y. Liu1, C. Gao1, Y.G. Cui1, J.Y. Liu1
1Nanjing Medical University, Center of Clinical Reproductive Medicine, Nanjing CityJiangsu Province, China
P-622 An association between thrombophilias and pregnancy loss: Should we test?
S. Bristow1, S. Yarnall1, A. Bisignano2, S. Munne3
1Recombine, Product, New York NY, U.S.A. 2Recombine, CEO, New York NY, U.S.A. 3Reprogenetics, Founder, Livingston NJ, U.S.A.
P-623 Preimplantation genetic diagnosis (PGD) for fragile X (FX) syndrome: direct allele repeat size detection and advantages of blastocyst stage biopsy
R. Prates1, M. Konstantinidis2, A. Jordan3, B. Chu2, E. Armenti3, T. Lemma2, V. Tecson2, S. Munne4, S. Jaroudi4
1Reprogenetics, Molecular, Miami, U.S.A. 2Reprogenetics, Molecular, Livingston, U.S.A. 3Reprogenetics, Genetic Counseling, Livingston, U.S.A. 4Reprogenetics, Research, Livingston, U.S.A.
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