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Sandra Janssens

Showing results (61-70 of 79) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 10, 2021
Outcome of publicly funded nationwide first-tier noninvasive prenatal screeningKris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Prenatal Diagnosis|October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Human Mutation|August 8, 2018
LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.
American Journal of Medical Genetics. Part A|October 1, 2015
Recurrent duplications of 17q12 associated with variable phenotypesElyse Mitchell, Andrew Douglas, Susanne Kjaegaard, et al.
European Journal of Medical Genetics|February 19, 2014
Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challengesOlivier Vanakker, Catheline Vilain, Katrien Janssens, et al.
Obstetrics and Gynecology|May 6, 2021
Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple GestationsMargot van Riel, Nathalie Brison, Machteld Baetens, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Genotype-phenotype analysis of the branchio-oculo-facial syndromeJeff M Milunsky, Tom M Maher, Geping Zhao, et al.
JAMA Neurology|February 14, 2018
Interpreting Genetic Variants in Titin in Patients With Muscle DisordersMarco Savarese, Lorenzo Maggi, Anna Vihola, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohortsMartina Marangoni, Guillaume Smits, Gilles Ceysens, et al.
Neurology|June 10, 2016
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patientsMarco Savarese, Giuseppina Di Fruscio, Annalaura Torella, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 10, 2021
Outcome of publicly funded nationwide first-tier noninvasive prenatal screeningKris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Prenatal Diagnosis|October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Human Mutation|August 8, 2018
LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.
American Journal of Medical Genetics. Part A|October 1, 2015
Recurrent duplications of 17q12 associated with variable phenotypesElyse Mitchell, Andrew Douglas, Susanne Kjaegaard, et al.
European Journal of Medical Genetics|February 19, 2014
Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challengesOlivier Vanakker, Catheline Vilain, Katrien Janssens, et al.
Obstetrics and Gynecology|May 6, 2021
Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple GestationsMargot van Riel, Nathalie Brison, Machteld Baetens, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Genotype-phenotype analysis of the branchio-oculo-facial syndromeJeff M Milunsky, Tom M Maher, Geping Zhao, et al.
JAMA Neurology|February 14, 2018
Interpreting Genetic Variants in Titin in Patients With Muscle DisordersMarco Savarese, Lorenzo Maggi, Anna Vihola, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohortsMartina Marangoni, Guillaume Smits, Gilles Ceysens, et al.
Neurology|June 10, 2016
The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patientsMarco Savarese, Giuseppina Di Fruscio, Annalaura Torella, et al.
Pageof 8