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Koen Devriendt

Showing results (61-70 of 183) with videos related to

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The Journal of Experimental Medicine|February 6, 2004
GATA-3 in human T cell helper type 2 developmentAlla Skapenko, Jan Leipe, Uwe Niesner, et al.
Prenatal Diagnosis|July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencingMolka Kammoun, Erika Souche, Paul Brady, et al.
Circulation|February 9, 2005
Novel mutation in the Per-Arnt-Sim domain of KCNH2 causes a malignant form of long-QT syndromeTom Rossenbacker, Kanigula Mubagwa, Roselie J Jongbloed, et al.
Clinical Dysmorphology|July 21, 2009
Congenital anterolateral bowing of the tibia with ipsilateral polydactyly of the great toe associated with cerebral cyst: a new entity?Jeroen Breckpot, Bernard Thienpont, Christine Vanhole, et al.
Clinical Genetics|February 6, 2020
LEF1 haploinsufficiency causes ectodermal dysplasiaJonathan Lévy, Yline Capri, Myriam Rachid, et al.
BMC Public Health|July 30, 2014
From the set-up of a screening program of breast cancer patients to the identification of the first BRCA mutation in the DR CongoGertrude Luyeye Mvila, Sandra Postema, Guy Marchal, et al.
European Journal of Medical Genetics|September 24, 2009
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Bernard Thienpont, Eftychia Dimitriadou, Katerina Theodoropoulos, et al.
Prenatal Diagnosis|April 29, 2017
Clinically relevant discordances identified after tertiary reassessment of fetuses with isolated congenital diaphragmatic herniaElisa Done, Leonardo Gucciardo, Tim Van Mieghem, et al.
Prenatal Diagnosis|August 18, 2021
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, et al.
Genome Medicine|April 10, 2026
Longitudinal cell-free DNA methylome and fragmentome profiles in health uncover signatures of cell type and demographic originMio Aerden, Tatjana Jatsenko, Kaat Leroy, et al.
Pageof 19

Showing results (61-70 of 183) with videos related to

Sort By:
Pageof 19
The Journal of Experimental Medicine|February 6, 2004
GATA-3 in human T cell helper type 2 developmentAlla Skapenko, Jan Leipe, Uwe Niesner, et al.
Prenatal Diagnosis|July 3, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencingMolka Kammoun, Erika Souche, Paul Brady, et al.
Circulation|February 9, 2005
Novel mutation in the Per-Arnt-Sim domain of KCNH2 causes a malignant form of long-QT syndromeTom Rossenbacker, Kanigula Mubagwa, Roselie J Jongbloed, et al.
Clinical Dysmorphology|July 21, 2009
Congenital anterolateral bowing of the tibia with ipsilateral polydactyly of the great toe associated with cerebral cyst: a new entity?Jeroen Breckpot, Bernard Thienpont, Christine Vanhole, et al.
Clinical Genetics|February 6, 2020
LEF1 haploinsufficiency causes ectodermal dysplasiaJonathan Lévy, Yline Capri, Myriam Rachid, et al.
BMC Public Health|July 30, 2014
From the set-up of a screening program of breast cancer patients to the identification of the first BRCA mutation in the DR CongoGertrude Luyeye Mvila, Sandra Postema, Guy Marchal, et al.
European Journal of Medical Genetics|September 24, 2009
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Bernard Thienpont, Eftychia Dimitriadou, Katerina Theodoropoulos, et al.
Prenatal Diagnosis|April 29, 2017
Clinically relevant discordances identified after tertiary reassessment of fetuses with isolated congenital diaphragmatic herniaElisa Done, Leonardo Gucciardo, Tim Van Mieghem, et al.
Prenatal Diagnosis|August 18, 2021
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, et al.
Genome Medicine|April 10, 2026
Longitudinal cell-free DNA methylome and fragmentome profiles in health uncover signatures of cell type and demographic originMio Aerden, Tatjana Jatsenko, Kaat Leroy, et al.
Pageof 19