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Koen Devriendt

Showing results (71-80 of 183) with videos related to

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European Journal of Medical Genetics|March 1, 2014
Presenting symptoms in adults with the 22q11 deletion syndromeAnnick Vogels, Sara Schevenels, Richard Cayenberghs, et al.
Human Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.
European Journal of Human Genetics : EJHG|February 10, 2007
Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autismDries Castermans, Joris R Vermeesch, Jean-Pierre Fryns, et al.
Heart Rhythm|April 27, 2005
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac deathTom Rossenbacker, Sheila J Carroll, Huajun Liu, et al.
Prenatal Diagnosis|August 18, 2023
What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores?Lore Lannoo, Joke Van Camp, Nathalie Brison, et al.
European Heart Journal|March 27, 2007
Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patientsBernard Thienpont, Luc Mertens, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
European Journal of Pediatrics|February 24, 2005
Tight skin and limited joint movements as early presentation of Hutchinson-Gilford progeria in a 7-week-old infantLieve Sevenants, Carine Wouters, Annachiara De Sandre-Giovannoli, et al.
Human Molecular Genetics|May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosisHilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
NPJ Genomic Medicine|July 10, 2019
Fetal sex determination in twin pregnancies using non-invasive prenatal testingDarine Villela, Huiwen Che, Marijke Van Ghelue, et al.
Pageof 19

Showing results (71-80 of 183) with videos related to

Sort By:
Pageof 19
European Journal of Medical Genetics|March 1, 2014
Presenting symptoms in adults with the 22q11 deletion syndromeAnnick Vogels, Sara Schevenels, Richard Cayenberghs, et al.
Human Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.
European Journal of Human Genetics : EJHG|February 10, 2007
Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autismDries Castermans, Joris R Vermeesch, Jean-Pierre Fryns, et al.
Heart Rhythm|April 27, 2005
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac deathTom Rossenbacker, Sheila J Carroll, Huajun Liu, et al.
Prenatal Diagnosis|August 18, 2023
What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores?Lore Lannoo, Joke Van Camp, Nathalie Brison, et al.
European Heart Journal|March 27, 2007
Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patientsBernard Thienpont, Luc Mertens, Thomy de Ravel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
European Journal of Pediatrics|February 24, 2005
Tight skin and limited joint movements as early presentation of Hutchinson-Gilford progeria in a 7-week-old infantLieve Sevenants, Carine Wouters, Annachiara De Sandre-Giovannoli, et al.
Human Molecular Genetics|May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosisHilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
NPJ Genomic Medicine|July 10, 2019
Fetal sex determination in twin pregnancies using non-invasive prenatal testingDarine Villela, Huiwen Che, Marijke Van Ghelue, et al.
Pageof 19