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Koenraad Devriendt

Showing results (51-60 of 190) with videos related to

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Plos One|May 14, 2009
Network analysis of differential expression for the identification of disease-causing genesDaniela Nitsch, Léon-Charles Tranchevent, Bernard Thienpont, et al.
European Journal of Medical Genetics|August 8, 2020
Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactylyMio Aerden, Marijke Bauters, Kris Van Den Bogaert, et al.
Clinical Case Reports|March 26, 2016
Williams-Beuren syndrome: pitfalls for diagnosis in limited resources settingAimé Lumaka, Rita Lukoo, Gerrye Mubungu, et al.
Frontiers in Genetics|June 6, 2018
Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical ExperienceSimon Ardui, Valerie Race, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part A|January 7, 2009
Elements of morphology: standard terminology for the lips, mouth, and oral regionJohn C Carey, M Michael Cohen, Cynthia J R Curry, et al.
American Journal of Medical Genetics. Part A|August 20, 2022
Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population-specific measurementsGerrye Mubungu, Mathieu Roelants, Aimé Lumaka, et al.
Bioinformatics (Oxford, England)|October 11, 2012
An unbiased evaluation of gene prioritization toolsDaniela Börnigen, Léon-Charles Tranchevent, Francisco Bonachela-Capdevila, et al.
American Journal of Medical Genetics. Part A|January 13, 2019
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndromeAnnelore Willaert, Charlotte Van Eynde, Nicolas Verhaert, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndromeElke Loos, Nicolas Verhaert, Annelore Willaert, et al.
American Journal of Medical Genetics. Part A|September 19, 2012
Atypical findings in three patients with Pai syndrome and literature reviewDamien Lederer, Brian Wilson, Pierre Lefesvre, et al.
Pageof 19

Showing results (51-60 of 190) with videos related to

Sort By:
Pageof 19
Plos One|May 14, 2009
Network analysis of differential expression for the identification of disease-causing genesDaniela Nitsch, Léon-Charles Tranchevent, Bernard Thienpont, et al.
European Journal of Medical Genetics|August 8, 2020
Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactylyMio Aerden, Marijke Bauters, Kris Van Den Bogaert, et al.
Clinical Case Reports|March 26, 2016
Williams-Beuren syndrome: pitfalls for diagnosis in limited resources settingAimé Lumaka, Rita Lukoo, Gerrye Mubungu, et al.
Frontiers in Genetics|June 6, 2018
Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical ExperienceSimon Ardui, Valerie Race, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part A|January 7, 2009
Elements of morphology: standard terminology for the lips, mouth, and oral regionJohn C Carey, M Michael Cohen, Cynthia J R Curry, et al.
American Journal of Medical Genetics. Part A|August 20, 2022
Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population-specific measurementsGerrye Mubungu, Mathieu Roelants, Aimé Lumaka, et al.
Bioinformatics (Oxford, England)|October 11, 2012
An unbiased evaluation of gene prioritization toolsDaniela Börnigen, Léon-Charles Tranchevent, Francisco Bonachela-Capdevila, et al.
American Journal of Medical Genetics. Part A|January 13, 2019
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndromeAnnelore Willaert, Charlotte Van Eynde, Nicolas Verhaert, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndromeElke Loos, Nicolas Verhaert, Annelore Willaert, et al.
American Journal of Medical Genetics. Part A|September 19, 2012
Atypical findings in three patients with Pai syndrome and literature reviewDamien Lederer, Brian Wilson, Pierre Lefesvre, et al.
Pageof 19