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David S Cram

Showing results (31-40 of 74) with videos related to

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Prenatal Diagnosis|February 3, 2016
Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencingXiangyu Zhu, Jie Li, Tong Ru, et al.
Life (Basel, Switzerland)|February 2, 2021
A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal SamplesXiya Zhou, Xiangbin Chen, Yulin Jiang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 14, 2014
A patient with five chromosomal rearrangements and a 2q31.1 microdeletionTing Wang, Jun Mao, Min-Juan Liu, et al.
Prenatal Diagnosis|December 18, 2015
Detection and quantitation of chromosomal mosaicism in human blastocysts using copy number variation sequencingTida Ruttanajit, Sujin Chanchamroen, David S Cram, et al.
Reproductive Biomedicine Online|May 20, 2015
The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryosJunmei Fan, Li Wang, Hui Wang, et al.
Reproductive Biomedicine Online|May 7, 2014
A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosisChong Chen, David S Cram, Fanni Xie, et al.
Oncotarget|July 14, 2016
Comprehensive profiling and quantitation of oncogenic mutations in non small-cell lung carcinoma using single molecule amplification and re-sequencing technologyShirong Zhang, Bing Xia, Hong Jiang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 28, 2014
A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosisHui Wang, Li Wang, Minyue Ma, et al.
Prenatal Diagnosis|April 17, 2016
Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluidQingwei Qi, Sijia Lu, Xiya Zhou, et al.
Reproductive Biomedicine Online|December 3, 2016
Corrigendum to 'A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis' [Reproductive BioMedicine Online 29 (2014) 136-139]Chong Chen, David S Cram, Fanni Xie, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|February 3, 2016
Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencingXiangyu Zhu, Jie Li, Tong Ru, et al.
Life (Basel, Switzerland)|February 2, 2021
A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal SamplesXiya Zhou, Xiangbin Chen, Yulin Jiang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 14, 2014
A patient with five chromosomal rearrangements and a 2q31.1 microdeletionTing Wang, Jun Mao, Min-Juan Liu, et al.
Prenatal Diagnosis|December 18, 2015
Detection and quantitation of chromosomal mosaicism in human blastocysts using copy number variation sequencingTida Ruttanajit, Sujin Chanchamroen, David S Cram, et al.
Reproductive Biomedicine Online|May 20, 2015
The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryosJunmei Fan, Li Wang, Hui Wang, et al.
Reproductive Biomedicine Online|May 7, 2014
A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosisChong Chen, David S Cram, Fanni Xie, et al.
Oncotarget|July 14, 2016
Comprehensive profiling and quantitation of oncogenic mutations in non small-cell lung carcinoma using single molecule amplification and re-sequencing technologyShirong Zhang, Bing Xia, Hong Jiang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 28, 2014
A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosisHui Wang, Li Wang, Minyue Ma, et al.
Prenatal Diagnosis|April 17, 2016
Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluidQingwei Qi, Sijia Lu, Xiya Zhou, et al.
Reproductive Biomedicine Online|December 3, 2016
Corrigendum to 'A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis' [Reproductive BioMedicine Online 29 (2014) 136-139]Chong Chen, David S Cram, Fanni Xie, et al.
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