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Annual Review of Genomics and Human Genetics
|
May 24, 2015
The Genetics of Soft Connective Tissue Disorders
Olivier Vanakker, Bert Callewaert, Fransiska Malfait, et al.
Methods in Molecular Medicine
|
August 26, 2006
Mutation analysis of the FBN1 gene in patients with Marfan syndrome
Paul Coucke, Petra Van Acker, Anne De Paepe
Scientific Reports
|
December 4, 2019
Nucleic acids enrichment of fungal pathogens to study host-pathogen interactions
Antonio Rodríguez, Brecht Guillemyn, Paul Coucke, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
August 29, 2018
BATCH-GE: Analysis of NGS Data for Genome Editing Assessment
Wouter Steyaert, Annekatrien Boel, Paul Coucke, et al.
Scientific Reports
|
July 1, 2025
How sample handling distorts telomere studies
Tijs K Tournoy, Dries S Martens, Julie De Backer, et al.
The Journal of Investigative Dermatology
|
October 2, 2025
The importance of being earnest: putting molecular analysis for the diagnosis of pseudoxanthoma elasticum in perspective
Shana Verschuere, Sofie Symoens, Delfien Syx, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2012
Spondyloperipheral dysplasia as the mosaic form of platyspondylic lethal skeletal dyplasia torrance type in mother and fetus with the same COL2A1 mutation
Julie Désir, Marie Cassart, Catherine Donner, et al.
Human Mutation
|
December 8, 2004
The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients
Fransiska Malfait, Paul Coucke, Sofie Symoens, et al.
Current Pharmaceutical Biotechnology
|
June 18, 2019
Comprehensive in silico Study of GLUT10: Prediction of Possible Substrate Binding Sites and Interacting Molecules
Mohammad J Hosen, Mahmudul Hasan, Sourav Chakraborty, et al.
Polskie Archiwum Medycyny Wewnetrznej
|
December 18, 2013
New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections
Laurence Campens, Marjolijn Renard, Bert Callewaert, et al.
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of 10
Search research articles
Search
Showing results (1-10 of 92) with videos related to
Sort By:
Page
of 10
Annual Review of Genomics and Human Genetics
|
May 24, 2015
The Genetics of Soft Connective Tissue Disorders
Olivier Vanakker, Bert Callewaert, Fransiska Malfait, et al.
Methods in Molecular Medicine
|
August 26, 2006
Mutation analysis of the FBN1 gene in patients with Marfan syndrome
Paul Coucke, Petra Van Acker, Anne De Paepe
Scientific Reports
|
December 4, 2019
Nucleic acids enrichment of fungal pathogens to study host-pathogen interactions
Antonio Rodríguez, Brecht Guillemyn, Paul Coucke, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
August 29, 2018
BATCH-GE: Analysis of NGS Data for Genome Editing Assessment
Wouter Steyaert, Annekatrien Boel, Paul Coucke, et al.
Scientific Reports
|
July 1, 2025
How sample handling distorts telomere studies
Tijs K Tournoy, Dries S Martens, Julie De Backer, et al.
The Journal of Investigative Dermatology
|
October 2, 2025
The importance of being earnest: putting molecular analysis for the diagnosis of pseudoxanthoma elasticum in perspective
Shana Verschuere, Sofie Symoens, Delfien Syx, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2012
Spondyloperipheral dysplasia as the mosaic form of platyspondylic lethal skeletal dyplasia torrance type in mother and fetus with the same COL2A1 mutation
Julie Désir, Marie Cassart, Catherine Donner, et al.
Human Mutation
|
December 8, 2004
The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients
Fransiska Malfait, Paul Coucke, Sofie Symoens, et al.
Current Pharmaceutical Biotechnology
|
June 18, 2019
Comprehensive in silico Study of GLUT10: Prediction of Possible Substrate Binding Sites and Interacting Molecules
Mohammad J Hosen, Mahmudul Hasan, Sourav Chakraborty, et al.
Polskie Archiwum Medycyny Wewnetrznej
|
December 18, 2013
New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections
Laurence Campens, Marjolijn Renard, Bert Callewaert, et al.
Page
of 10