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Cancer Research
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October 5, 2016
β-Catenin Mutations: Insights into the APC Pathway and the Power of Genetics
Patrice J Morin, Kenneth W Kinzler, Andrew B Sparks
American Journal of Obstetrics and Gynecology
|
April 3, 2012
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18
Andrew B Sparks, Craig A Struble, Eric T Wang, et al.
Nature Biotechnology
|
May 1, 2002
Using the transcriptome to annotate the genome
Saurabh Saha, Andrew B Sparks, Carlo Rago, et al.
Prenatal Diagnosis
|
January 7, 2012
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy
Andrew B Sparks, Eric T Wang, Craig A Struble, et al.
American Journal of Obstetrics and Gynecology
|
June 30, 2012
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
Mary E Norton, Herb Brar, Jonathan Weiss, et al.
Nature
|
May 28, 2010
The mutation spectrum revealed by paired genome sequences from a lung cancer patient
William Lee, Zhaoshi Jiang, Jinfeng Liu, et al.
Nature
|
July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
Brock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Science (New York, N.Y.)
|
October 13, 2007
The genomic landscapes of human breast and colorectal cancers
Laura D Wood, D Williams Parsons, Siân Jones, et al.
Science (New York, N.Y.)
|
November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
Radoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Cancer Research
|
October 5, 2016
β-Catenin Mutations: Insights into the APC Pathway and the Power of Genetics
Patrice J Morin, Kenneth W Kinzler, Andrew B Sparks
American Journal of Obstetrics and Gynecology
|
April 3, 2012
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18
Andrew B Sparks, Craig A Struble, Eric T Wang, et al.
Nature Biotechnology
|
May 1, 2002
Using the transcriptome to annotate the genome
Saurabh Saha, Andrew B Sparks, Carlo Rago, et al.
Prenatal Diagnosis
|
January 7, 2012
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy
Andrew B Sparks, Eric T Wang, Craig A Struble, et al.
American Journal of Obstetrics and Gynecology
|
June 30, 2012
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
Mary E Norton, Herb Brar, Jonathan Weiss, et al.
Nature
|
May 28, 2010
The mutation spectrum revealed by paired genome sequences from a lung cancer patient
William Lee, Zhaoshi Jiang, Jinfeng Liu, et al.
Nature
|
July 13, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
Brock A Peters, Bahram G Kermani, Andrew B Sparks, et al.
Science (New York, N.Y.)
|
October 13, 2007
The genomic landscapes of human breast and colorectal cancers
Laura D Wood, D Williams Parsons, Siân Jones, et al.
Science (New York, N.Y.)
|
November 7, 2009
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
Radoje Drmanac, Andrew B Sparks, Matthew J Callow, et al.
Page
of 1