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Molecular Human Reproduction
|
December 24, 2010
Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses
Nathan R Treff, Jing Su, Xin Tao, et al.
Experimental Cell Research
|
May 17, 2005
Dynamic mitochondrial localization of nuclear transcription factor HMGA1
Gregory A Dement, Nathan R Treff, Nancy S Magnuson, et al.
Fertility and Sterility
|
December 6, 2025
Accuracy of Direct Mutation Testing by TaqMan qPCR for Preimplantation Genetic Diagnosis of Recurrent de Novo Mutations
Diana Garro, Jia Xu, Deirdre Leahy, et al.
Fertility and Sterility
|
June 19, 2013
Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial
Richard T Scott, Kathleen M Upham, Eric J Forman, et al.
Fertility and Sterility
|
February 7, 2012
Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study
Richard T Scott, Kathleen Ferry, Jing Su, et al.
Reproduction (Cambridge, England)
|
May 16, 2020
PREIMPLANTATION GENETIC TESTING: Preimplantation genetic testing for polygenic disease risk
Nathan R Treff, Diego Marin, Louis Lello, et al.
Reproductive Biomedicine Online
|
January 26, 2018
Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts
Diego Marin, Rebekah Zimmerman, Xin Tao, et al.
Fertility and Sterility
|
January 15, 2013
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease
Nathan R Treff, Anastasia Fedick, Xin Tao, et al.
Molecular Genetics & Genomic Medicine
|
March 25, 2015
Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population
Anastasia M Fedick, Chaim Jalas, Nathan R Treff, et al.
Journal of Assisted Reproduction and Genetics
|
August 8, 2014
Improved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD
Ndeye-Aicha Gueye, Chaim Jalas, Xin Tao, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 98) with videos related to
Sort By:
Page
of 10
Molecular Human Reproduction
|
December 24, 2010
Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses
Nathan R Treff, Jing Su, Xin Tao, et al.
Experimental Cell Research
|
May 17, 2005
Dynamic mitochondrial localization of nuclear transcription factor HMGA1
Gregory A Dement, Nathan R Treff, Nancy S Magnuson, et al.
Fertility and Sterility
|
December 6, 2025
Accuracy of Direct Mutation Testing by TaqMan qPCR for Preimplantation Genetic Diagnosis of Recurrent de Novo Mutations
Diana Garro, Jia Xu, Deirdre Leahy, et al.
Fertility and Sterility
|
June 19, 2013
Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial
Richard T Scott, Kathleen M Upham, Eric J Forman, et al.
Fertility and Sterility
|
February 7, 2012
Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study
Richard T Scott, Kathleen Ferry, Jing Su, et al.
Reproduction (Cambridge, England)
|
May 16, 2020
PREIMPLANTATION GENETIC TESTING: Preimplantation genetic testing for polygenic disease risk
Nathan R Treff, Diego Marin, Louis Lello, et al.
Reproductive Biomedicine Online
|
January 26, 2018
Validation of a targeted next generation sequencing-based comprehensive chromosome screening platform for detection of triploidy in human blastocysts
Diego Marin, Rebekah Zimmerman, Xin Tao, et al.
Fertility and Sterility
|
January 15, 2013
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease
Nathan R Treff, Anastasia Fedick, Xin Tao, et al.
Molecular Genetics & Genomic Medicine
|
March 25, 2015
Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population
Anastasia M Fedick, Chaim Jalas, Nathan R Treff, et al.
Journal of Assisted Reproduction and Genetics
|
August 8, 2014
Improved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD
Ndeye-Aicha Gueye, Chaim Jalas, Xin Tao, et al.
Page
of 10