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Clinical Genetics
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March 28, 2024
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis
Christian M Parobek, Roni Zemet, Matthew A Shanahan, et al.
Stem Cells and Development
|
July 9, 2013
Influence of activin A supplementation during human embryonic stem cell derivation on germ cell differentiation potential
Galbha Duggal, Björn Heindryckx, Sharat Warrier, et al.
Prenatal Diagnosis
|
May 27, 2025
Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth
Roni Zemet, Christian M Parobek, April D Adams, et al.
Proteomics
|
July 10, 2016
Assessing the impact of minimizing arginine conversion in fully defined SILAC culture medium in human embryonic stem cells
Ellen Scheerlinck, Katleen Van Steendam, Simon Daled, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 20, 2023
Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory
Linyan Meng, Ruben Attali, Tomer Talmy, et al.
Molecular Genetics and Metabolism
|
January 9, 2025
Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes
Charles R DiFalco, Charul Gijavanekar, Yue Wang, et al.
Analytical Biochemistry
|
June 10, 2014
Detailed method description for noninvasive monitoring of differentiation status of human embryonic stem cells
Ellen Scheerlinck, Katleen Van Steendam, Mado Vandewoestyne, et al.
Prenatal Diagnosis
|
October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Clinical Chemistry
|
January 3, 2025
Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage
Matthew Hoi Kin Chau, Stephanie A Anderson, Rodger Song, et al.
American Journal of Human Genetics
|
December 2, 2019
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Clinical Genetics
|
March 28, 2024
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis
Christian M Parobek, Roni Zemet, Matthew A Shanahan, et al.
Stem Cells and Development
|
July 9, 2013
Influence of activin A supplementation during human embryonic stem cell derivation on germ cell differentiation potential
Galbha Duggal, Björn Heindryckx, Sharat Warrier, et al.
Prenatal Diagnosis
|
May 27, 2025
Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth
Roni Zemet, Christian M Parobek, April D Adams, et al.
Proteomics
|
July 10, 2016
Assessing the impact of minimizing arginine conversion in fully defined SILAC culture medium in human embryonic stem cells
Ellen Scheerlinck, Katleen Van Steendam, Simon Daled, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 20, 2023
Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory
Linyan Meng, Ruben Attali, Tomer Talmy, et al.
Molecular Genetics and Metabolism
|
January 9, 2025
Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes
Charles R DiFalco, Charul Gijavanekar, Yue Wang, et al.
Analytical Biochemistry
|
June 10, 2014
Detailed method description for noninvasive monitoring of differentiation status of human embryonic stem cells
Ellen Scheerlinck, Katleen Van Steendam, Mado Vandewoestyne, et al.
Prenatal Diagnosis
|
October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Clinical Chemistry
|
January 3, 2025
Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage
Matthew Hoi Kin Chau, Stephanie A Anderson, Rodger Song, et al.
American Journal of Human Genetics
|
December 2, 2019
Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis
Liesbeth Vossaert, Qun Wang, Roseen Salman, et al.
Page
of 4