Canlyniadau Chwilio - Treff, Nathan R

Methods for comprehensive chromosome screening of oocytes and embryos: capabilities, limitations, and evidence of validity gan Treff, Nathan R., Scott, Richard T.

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Editorial: Causes of Oocyte Aneuploidy and Infertility in Advanced Maternal Age and Emerging Therapeutic Approaches gan Bernstein, Lori R., Treff, Nathan R.

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Isn’t it time to stop calling preimplantation embryos “mosaic”? gan Paulson, Richard J., Treff, Nathan R.

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Preimplantation genetic testing for aneuploidy: A review of published blastocyst reanalysis concordance data gan Marin, Diego, Xu, Jia, Treff, Nathan R.

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Telomere DNA Deficiency Is Associated with Development of Human Embryonic Aneuploidy gan Treff, Nathan R., Su, Jing, Taylor, Deanne, Scott, Richard T.

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High-throughput real-time PCR-based genotyping without DNA purification gan Fedick, Anastasia, Su, Jing, Jalas, Chaim, Treff, Nathan R

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Comprehensive chromosome screening and gene expression analysis from the same biopsy in human preimplantation embryos gan Marin, Diego, Wang, Yujue, Tao, Xin, Scott, Richard T., Treff, Nathan R.

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Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses gan Treff, Nathan R., Su, Jing, Tao, Xin, Northrop, Lesley E., Scott, Richard T.

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SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH gan Treff, Nathan R., Levy, Brynn, Su, Jing, Northrop, Lesley E., Tao, Xin, Scott, Richard T.

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Improved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD gan Gueye, Ndeye-Aicha, Jalas, Chaim, Tao, Xin, Taylor, Deanne, Scott, Richard T., Treff, Nathan R.

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Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population gan Fedick, Anastasia M, Jalas, Chaim, Treff, Nathan R, Knowles, Michael R, Zariwala, Maimoona A

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High-Throughput Carrier Screening Using TaqMan Allelic Discrimination gan Fedick, Anastasia, Su, Jing, Jalas, Chaim, Northrop, Lesley, Devkota, Batsal, Ekstein, Josef, Treff, Nathan R.

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Expression and characterization of three Aurora kinase C splice variants found in human oocytes gan Fellmeth, Jessica E., Gordon, Derek, Robins, Christian E., Scott, Richard T., Treff, Nathan R., Schindler, Karen

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Polar body morphology is not predictive of its cell division origin gan Treff, Nathan R., Scott, Richard T., Su, Jing, Campos, Jessyca, Stevens, John, Schoolcraft, William, Katz-Jaffe, Mandy

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Embryo Screening for Polygenic Disease Risk: Recent Advances and Ethical Considerations gan Tellier, Laurent C. A. M., Eccles, Jennifer, Treff, Nathan R., Lello, Louis, Fishel, Simon, Hsu, Stephen

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Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocysts gan Treff, Nathan R., Forman, Eric J., Katz-Jaffe, Mandy G., Schoolcraft, William B., Levy, Brynn, Scott, Richard T.

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Trophectoderm DNA fingerprinting by quantitative real-time PCR successfully distinguishes sibling human embryos gan Scott, Richard T., Su, Jing, Tao, Xin, Forman, Eric J., Hong, Kathleen H., Taylor, Deanne, Treff, Nathan R.

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Comparison of array comparative genomic hybridization and quantitative real-time PCR-based aneuploidy screening of blastocyst biopsies gan Capalbo, Antonio, Treff, Nathan R, Cimadomo, Danilo, Tao, Xin, Upham, Kathleen, Ubaldi, Filippo Maria, Rienzi, Laura, Scott, Richard T

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Lack of association of KATNAL1 gene sequence variants and azoospermia in humans gan Fedick, Anastasia M., Eckert, Kyle, Thompson, Katharine, Forman, Eric J., Devkota, Batsal, Treff, Nathan R., Taylor, Deanne, Scott, Richard T.

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Evaluation of comprehensive chromosome screening platforms for the detection of mosaic segmental aneuploidy gan Goodrich, David, Xing, Tongji, Tao, Xin, Lonczak, Agnieszka, Zhan, Yiping, Landis, Jessica, Zimmerman, Rebekah, Scott, Richard T., Treff, Nathan R.

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