Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations von Wang, Li, Shen, Jiandong, Cram, David S., Ma, Minyue, Wang, Hui, Zhang, Wenke, Fan, Junmei, Gao, Zhiying, Zhang, Liwen, Li, Zhifeng, Xu, Mengnan, Leigh, Don A., Trounson, Alan O., Liu, Jiayin, Yao, Yuanqing

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Pregnancies and live births after trophectoderm biopsy and preimplantation genetic testing of human blastocysts von McArthur, Steven J., Leigh, Don, Marshall, James T., de Boer, Kylie A., Jansen, Robert P.S.

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PROGRESS TOWARDS UNIVERSAL PGT- HOW CLOSE ARE WE TO COMPREHENSIVE PGT? von Leigh, Don

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Improvement and standardization of biopsy procedures von Leigh, Don

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What next for preimplantation genetic screening (PGS)? Experience with blastocyst biopsy and testing for aneuploidy von Jansen, Robert P.S., Bowman, Mark C., de Boer, Kylie A., Leigh, Don A., Lieberman, Devora B., McArthur, Steven J.

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It's a mosaic result- what do I say now? von Leigh, Don

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UPDATED PGDIS RECOMMENDATIONS FOR REPLACEMENT OF MOSAIC EMBRYOS von Cram, David, Leigh, Don

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Moving to blastocyst biopsy for preimplantation genetic diagnosis and single embryo transfer at sydney IVF von de Boer, Kylie A, Catt, James W, Jansen, Robert P.S, Leigh, Don, McArthur, Steven

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Identification of a jumping translocation following pre-implantation genetic diagnosis von Carey, Louise, Traversa, Maria V., Wright, Dale C., McArthur, Steven J., Leigh, Don A.

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The uncertainty of copy number variants: pregnancy decisions and clinical follow-up von Shi, Panlai, Liang, Hongbin, Hou, Yaqin, Chen, Duo, Ren, Huanan, Wang, Conghui, Xia, Yanjie, Zhang, Da, Leigh, Don, Cram, David S., Kong, Xiangdong

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Third-generation sequencing: any future opportunities for PGT? von Liu, Sai, Wang, Hui, Leigh, Don, Cram, David S., Wang, Li, Yao, Yuanqing

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NIPT - POTENTIAL TOOL FOR PGT FOLLOW UP von Cram, David, Leigh, Don, Rechistsky, Svetlana, Kuliev, Anver

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Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups von M.M, Yanfei Cheng, Yu, Qian, Ma, Minyue, Wang, Hui, Tian, Shuang, Zhang, Wenling, M.M., Jinning Zhang, Liu, Yifan, Yang, Qi, Pan, Xiao, Liang, Hongbin, Wang, Li, Leigh, Don, Cram, David S., Yao, Yuanqing

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Mitochondrial DNA Levels are not a simple indicator for preselection of Euploid Embrios with higher developmental potential von Rechistsky, Svetlana, Cram, David, Leigh, Don, Cao, Yanan, Wang, Li, Yao, Yuanqing, Kuliev, Anver

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Single-Molecule Sequencing: A New Approach for Preimplantation Testing and Noninvasive Prenatal Diagnosis Confirmation of Fetal Genotype von Rechitsky, Svetlana, Kuliev, Anver, San Ramon, Geraldine, Tur-Kaspa, Ilan, Wang, Yin, Wang, Wenjie, Wu, Xueqing, Wang, Li, Leigh, Don, Cram, David S

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A New Approach for Preimplantation Testing and Noninvasive Prenatal Diagnosis Confirmation of Fetal Genotype von Rechitsky, Svetlana, Kuliev, Anver, San Ramon, Geraldine, Tur-Kaspa, Ilan, Wang, Yin, Wang, Wenjie, Wu, Xueqing, Wang, Li, Leigh, Don, Cram, David S.

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Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test von Carey, Louise, Scott, Fergus, Murphy, Kristi, Mansfield, Nerida, Barahona, Paulette, Leigh, Don, Robertson, Rob, McLennan, Andrew

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Single-Molecule Sequencing von Rechitsky, Svetlana, Kuliev, Anver, San Ramon, Geraldine, Tur-Kaspa, Ilan, Wang, Yin, Wang, Wenjie, Wu, Xueqing, Wang, Li, Leigh, Don, Cram, David S.

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Clinical application of single‐molecule optical mapping to a multigeneration FSHD1 pedigree von Zhang, Qian, Xu, Xueqin, Ding, Lirong, Li, Huanzheng, Xu, Chengyang, Gong, Yuyan, Liu, Ying, Mu, Ting, Leigh, Don, Cram, David S., Tang, Shaohua

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Universal Amplification of DNA Isolated from Small Regions of Paraffin-Embedded, Formalin-Fixed Tissue von Faulkner, Stefan W, Leigh, Don A

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