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Sandra Janssens

Showing results (21-30 of 79) with videos related to

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Journal of Medical Genetics|August 6, 2010
Developmental delay and connective tissue disorder in four patients sharing a common microdeletion at 6q13-14Hilde Van Esch, Elisabeth M Rosser, Sandra Janssens, et al.
Journal of Genetic Counseling|April 13, 2024
Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couplesAriane J A G Van Tongerloo, Hannah Verdin, Wouter Steyaert, et al.
BMC Medical Genetics|September 16, 2009
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samplesBjörn Menten, Katrien Swerts, Barbara Delle Chiaie, et al.
Research in Developmental Disabilities|August 23, 2014
Deficient motor timing in children with neurofibromatosis type 1Julie Debrabant, Ellen Plasschaert, Karen Caeyenberghs, et al.
European Journal of Human Genetics : EJHG|July 30, 2015
Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issuesSandra Janssens, Davit Chokoshvilli, Carmen Binst, et al.
Personalized Medicine|May 15, 2018
Attitudes of cystic fibrosis patients and their parents towards direct-to-consumer genetic testing for carrier statusSandra Janssens, Louiza Kalokairinou, Davit Chokoshvilli, et al.
Prenatal Diagnosis|May 14, 2016
Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratoryAnnelies Dheedene, Tom Sante, Matthias De Smet, et al.
Genetic Testing and Molecular Biomarkers|March 18, 2017
Public Views on Genetics and Genetic Testing: A Survey of the General Public in BelgiumDavit Chokoshvili, Carmen Belmans, Roxanne Poncelet, et al.
Genes|January 21, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?Thomas Clabout, Laurence Maes, Frederic Acke, et al.
American Journal of Human Genetics|August 2, 2007
Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1Ophélia Maertens, Sofie De Schepper, Jo Vandesompele, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|August 6, 2010
Developmental delay and connective tissue disorder in four patients sharing a common microdeletion at 6q13-14Hilde Van Esch, Elisabeth M Rosser, Sandra Janssens, et al.
Journal of Genetic Counseling|April 13, 2024
Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couplesAriane J A G Van Tongerloo, Hannah Verdin, Wouter Steyaert, et al.
BMC Medical Genetics|September 16, 2009
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samplesBjörn Menten, Katrien Swerts, Barbara Delle Chiaie, et al.
Research in Developmental Disabilities|August 23, 2014
Deficient motor timing in children with neurofibromatosis type 1Julie Debrabant, Ellen Plasschaert, Karen Caeyenberghs, et al.
European Journal of Human Genetics : EJHG|July 30, 2015
Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issuesSandra Janssens, Davit Chokoshvilli, Carmen Binst, et al.
Personalized Medicine|May 15, 2018
Attitudes of cystic fibrosis patients and their parents towards direct-to-consumer genetic testing for carrier statusSandra Janssens, Louiza Kalokairinou, Davit Chokoshvilli, et al.
Prenatal Diagnosis|May 14, 2016
Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratoryAnnelies Dheedene, Tom Sante, Matthias De Smet, et al.
Genetic Testing and Molecular Biomarkers|March 18, 2017
Public Views on Genetics and Genetic Testing: A Survey of the General Public in BelgiumDavit Chokoshvili, Carmen Belmans, Roxanne Poncelet, et al.
Genes|January 21, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?Thomas Clabout, Laurence Maes, Frederic Acke, et al.
American Journal of Human Genetics|August 2, 2007
Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1Ophélia Maertens, Sofie De Schepper, Jo Vandesompele, et al.
Pageof 8