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Bert de Vries

Showing results (11-20 of 21) with videos related to

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Entropy (Basel, Switzerland)|July 2, 2021
Variational Message Passing and Local Constraint Manipulation in Factor Graphsİsmail Şenöz, Thijs van de Laar, Dmitry Bagaev, et al.
American Journal of Medical Genetics. Part A|December 15, 2007
Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletionRaveen Shahdadpuri, Bert de Vries, Rolph Pfundt, et al.
Frontiers in Robotics and AI|April 25, 2022
Active Inference and Epistemic Value in Graphical ModelsThijs van de Laar, Magnus Koudahl, Bart van Erp, et al.
Entropy (Basel, Switzerland)|August 26, 2023
Automating Model Comparison in Factor GraphsBart van Erp, Wouter W L Nuijten, Thijs van de Laar, et al.
Genome Research|April 19, 2015
The clustering of functionally related genes contributes to CNV-mediated diseaseTallulah Andrews, Frantisek Honti, Rolph Pfundt, et al.
American Journal of Medical Genetics. Part A|November 22, 2012
Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndromeJos I M Egger, Ellen Wingbermühle, Willem M A Verhoeven, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiencyDespina Contopoulos-Ioannidis, Athanasios Evangeliou, Henk ter Laak, et al.
BMC Biotechnology|December 21, 2017
Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disabilityTracy Dudding-Byth, Anne Baxter, Elizabeth G Holliday, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysisIlse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema-Raddatz, et al.
Molecular Neurobiology|June 7, 2012
BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patientsAsma Tlili, Alexander Hoischen, Clémentine Ripoll, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Entropy (Basel, Switzerland)|July 2, 2021
Variational Message Passing and Local Constraint Manipulation in Factor Graphsİsmail Şenöz, Thijs van de Laar, Dmitry Bagaev, et al.
American Journal of Medical Genetics. Part A|December 15, 2007
Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletionRaveen Shahdadpuri, Bert de Vries, Rolph Pfundt, et al.
Frontiers in Robotics and AI|April 25, 2022
Active Inference and Epistemic Value in Graphical ModelsThijs van de Laar, Magnus Koudahl, Bart van Erp, et al.
Entropy (Basel, Switzerland)|August 26, 2023
Automating Model Comparison in Factor GraphsBart van Erp, Wouter W L Nuijten, Thijs van de Laar, et al.
Genome Research|April 19, 2015
The clustering of functionally related genes contributes to CNV-mediated diseaseTallulah Andrews, Frantisek Honti, Rolph Pfundt, et al.
American Journal of Medical Genetics. Part A|November 22, 2012
Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndromeJos I M Egger, Ellen Wingbermühle, Willem M A Verhoeven, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiencyDespina Contopoulos-Ioannidis, Athanasios Evangeliou, Henk ter Laak, et al.
BMC Biotechnology|December 21, 2017
Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disabilityTracy Dudding-Byth, Anne Baxter, Elizabeth G Holliday, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysisIlse Feenstra, Nicolien Hanemaaijer, Birgit Sikkema-Raddatz, et al.
Molecular Neurobiology|June 7, 2012
BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patientsAsma Tlili, Alexander Hoischen, Clémentine Ripoll, et al.
Pageof 3