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The Journal of Molecular Diagnostics : JMD
|
January 11, 2024
Detection of Constitutional Structural Variants by Optical Genome Mapping: A Multisite Study of Postnatal Samples
Ulrich Broeckel, M Anwar Iqbal, Brynn Levy, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2016
Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome
Jess F Peterson, David P Bick, Gabrielle C Geddes, et al.
Nature Communications
|
November 15, 2017
PLCγ-dependent mTOR signalling controls IL-7-mediated early B cell development
Mei Yu, Yuhong Chen, Hu Zeng, et al.
JAMA Cardiology
|
October 23, 2024
Utility of a Systolic Blood Pressure Polygenic Risk Score With Chlorthalidone Response
Nicole D Armstrong, Vinodh Srinivasasainagendra, Amit Patki, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
May 15, 2007
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations
Kamil Sedlacek, Katharina Neureuther, Jakob C Mueller, et al.
The Pharmacogenomics Journal
|
September 13, 2018
Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies
Katherine M Robinson, Wenjian Yang, Cyrine E Haidar, et al.
The Journal of Molecular Diagnostics : JMD
|
February 24, 2023
Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases
M Anwar Iqbal, Ulrich Broeckel, Brynn Levy, et al.
Physiological Genomics
|
June 17, 2010
Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease
Aoy Tomita-Mitchell, Donna K Mahnke, Joshua M Larson, et al.
Physiological Genomics
|
June 20, 2013
SORCS1 contributes to the development of renal disease in rats and humans
Jozef Lazar, Caitlin C O'Meara, Allison B Sarkis, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
December 27, 2011
Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertension
James P Maloney, Robert S Stearman, Todd M Bull, et al.
Page
of 13
Search research articles
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Showing results (61-70 of 125) with videos related to
Sort By:
Page
of 13
The Journal of Molecular Diagnostics : JMD
|
January 11, 2024
Detection of Constitutional Structural Variants by Optical Genome Mapping: A Multisite Study of Postnatal Samples
Ulrich Broeckel, M Anwar Iqbal, Brynn Levy, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2016
Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome
Jess F Peterson, David P Bick, Gabrielle C Geddes, et al.
Nature Communications
|
November 15, 2017
PLCγ-dependent mTOR signalling controls IL-7-mediated early B cell development
Mei Yu, Yuhong Chen, Hu Zeng, et al.
JAMA Cardiology
|
October 23, 2024
Utility of a Systolic Blood Pressure Polygenic Risk Score With Chlorthalidone Response
Nicole D Armstrong, Vinodh Srinivasasainagendra, Amit Patki, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
May 15, 2007
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations
Kamil Sedlacek, Katharina Neureuther, Jakob C Mueller, et al.
The Pharmacogenomics Journal
|
September 13, 2018
Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies
Katherine M Robinson, Wenjian Yang, Cyrine E Haidar, et al.
The Journal of Molecular Diagnostics : JMD
|
February 24, 2023
Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases
M Anwar Iqbal, Ulrich Broeckel, Brynn Levy, et al.
Physiological Genomics
|
June 17, 2010
Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease
Aoy Tomita-Mitchell, Donna K Mahnke, Joshua M Larson, et al.
Physiological Genomics
|
June 20, 2013
SORCS1 contributes to the development of renal disease in rats and humans
Jozef Lazar, Caitlin C O'Meara, Allison B Sarkis, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
December 27, 2011
Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertension
James P Maloney, Robert S Stearman, Todd M Bull, et al.
Page
of 13