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Koen Devriendt

Showing results (111-120 of 183) with videos related to

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The Lancet. Planetary Health|May 1, 2020
Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the CongoDaan Van Brusselen, Tony Kayembe-Kitenge, Sébastien Mbuyi-Musanzayi, et al.
Human Mutation|May 12, 2007
Subtelomeric imbalances in phenotypically normal individualsIrina Balikova, Björn Menten, Thomy de Ravel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2016
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidiesNathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, et al.
Human Molecular Genetics|October 14, 2006
Sesn1 is a novel gene for left-right asymmetry and mediating nodal signalingHilde Peeters, Marianne L Voz, Kristin Verschueren, et al.
Seminars in Fetal & Neonatal Medicine|November 17, 2009
Fetal surgery is a clinical realityJan A Deprest, Roland Devlieger, Kasemsri Srisupundit, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Plos Genetics|November 7, 2014
Pseudoautosomal region 1 length polymorphism in the human populationMartin A Mensah, Matthew S Hestand, Maarten H D Larmuseau, et al.
The Journal of Clinical Investigation|October 27, 2009
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in miceVictoria Randall, Karen McCue, Catherine Roberts, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders - the DDD-Africa studyNadja Louw, Prince Makay, Phelelani T Mpangase, et al.
Pageof 19

Showing results (111-120 of 183) with videos related to

Sort By:
Pageof 19
The Lancet. Planetary Health|May 1, 2020
Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the CongoDaan Van Brusselen, Tony Kayembe-Kitenge, Sébastien Mbuyi-Musanzayi, et al.
Human Mutation|May 12, 2007
Subtelomeric imbalances in phenotypically normal individualsIrina Balikova, Björn Menten, Thomy de Ravel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2016
Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidiesNathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, et al.
Human Molecular Genetics|October 14, 2006
Sesn1 is a novel gene for left-right asymmetry and mediating nodal signalingHilde Peeters, Marianne L Voz, Kristin Verschueren, et al.
Seminars in Fetal & Neonatal Medicine|November 17, 2009
Fetal surgery is a clinical realityJan A Deprest, Roland Devlieger, Kasemsri Srisupundit, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Plos Genetics|November 7, 2014
Pseudoautosomal region 1 length polymorphism in the human populationMartin A Mensah, Matthew S Hestand, Maarten H D Larmuseau, et al.
The Journal of Clinical Investigation|October 27, 2009
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in miceVictoria Randall, Karen McCue, Catherine Roberts, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders - the DDD-Africa studyNadja Louw, Prince Makay, Phelelani T Mpangase, et al.
Pageof 19