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Clinical Biochemistry
|
May 7, 2013
Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing
David Wong, Sharmili Moturi, Vach Angkachatchai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 2008
Cytosine methylation profiling of cancer cell lines
Mathias Ehrich, Julia Turner, Peter Gibbs, et al.
The Journal of Molecular Diagnostics : JMD
|
June 28, 2011
Restriction enzyme-mediated enhanced detection of circulating cell-free fetal DNA in maternal plasma
John A Tynan, Payam Mahboubi, Lesley L Cagasan, et al.
Nucleic Acids Research
|
April 25, 2003
RNase T1 mediated base-specific cleavage and MALDI-TOF MS for high-throughput comparative sequence analysis
Ralf Hartmer, Niels Storm, Sebastian Boecker, et al.
Blood
|
November 12, 2009
Quantitative DNA methylation predicts survival in adult acute myeloid leukemia
Lars Bullinger, Mathias Ehrich, Konstanze Döhner, et al.
Clinical Chemistry
|
February 22, 2013
A new era in prenatal diagnosis: the use of cell-free fetal DNA in maternal circulation for detection of chromosomal aneuploidies
Jennifer L Shea, Eleftherios P Diamandis, Barry Hoffman, et al.
Clinical Chemistry
|
August 24, 2010
Quantification of fetal DNA by use of methylation-based DNA discrimination
Anders O H Nygren, Jarrod Dean, Taylor J Jensen, et al.
Pharmacogenomics
|
February 27, 2013
Two algorithms for biospecimen comparison and differentiation using SNP genotypes
Scott Morris, Esma S Gel, Jordan V Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 12, 2002
Association testing by DNA pooling: an effective initial screen
Aruna Bansal, Dirk van den Boom, Stefan Kammerer, et al.
American Journal of Obstetrics and Gynecology
|
March 25, 2014
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA
Richard P Porreco, Thomas J Garite, Kimberly Maurel, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 61) with videos related to
Sort By:
Page
of 7
Clinical Biochemistry
|
May 7, 2013
Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing
David Wong, Sharmili Moturi, Vach Angkachatchai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 2008
Cytosine methylation profiling of cancer cell lines
Mathias Ehrich, Julia Turner, Peter Gibbs, et al.
The Journal of Molecular Diagnostics : JMD
|
June 28, 2011
Restriction enzyme-mediated enhanced detection of circulating cell-free fetal DNA in maternal plasma
John A Tynan, Payam Mahboubi, Lesley L Cagasan, et al.
Nucleic Acids Research
|
April 25, 2003
RNase T1 mediated base-specific cleavage and MALDI-TOF MS for high-throughput comparative sequence analysis
Ralf Hartmer, Niels Storm, Sebastian Boecker, et al.
Blood
|
November 12, 2009
Quantitative DNA methylation predicts survival in adult acute myeloid leukemia
Lars Bullinger, Mathias Ehrich, Konstanze Döhner, et al.
Clinical Chemistry
|
February 22, 2013
A new era in prenatal diagnosis: the use of cell-free fetal DNA in maternal circulation for detection of chromosomal aneuploidies
Jennifer L Shea, Eleftherios P Diamandis, Barry Hoffman, et al.
Clinical Chemistry
|
August 24, 2010
Quantification of fetal DNA by use of methylation-based DNA discrimination
Anders O H Nygren, Jarrod Dean, Taylor J Jensen, et al.
Pharmacogenomics
|
February 27, 2013
Two algorithms for biospecimen comparison and differentiation using SNP genotypes
Scott Morris, Esma S Gel, Jordan V Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 12, 2002
Association testing by DNA pooling: an effective initial screen
Aruna Bansal, Dirk van den Boom, Stefan Kammerer, et al.
American Journal of Obstetrics and Gynecology
|
March 25, 2014
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA
Richard P Porreco, Thomas J Garite, Kimberly Maurel, et al.
Page
of 7