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Personalized Medicine|May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticistsDavit Chokoshvili, Sandra Janssens, Danya Vears, et al.American Journal of Medical Genetics. Part A|August 28, 2010
Barber-Say syndrome in a father and daughterNathalie Roche, Philippe Houtmeyers, Sandra Janssens, et al.Journal of Medical Ethics|February 3, 2026
Risk management and the further use of gametes from a donor with a known pathogenic variantDorian Accoe, Guido Pennings, Sandra Janssens, et al.Journal of Voice : Official Journal of the Voice Foundation|May 10, 2011
Voice-related quality of life in adults with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.Journal of Fluency Disorders|September 14, 2010
Word-final prolongations in an adult male with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Paul Corthals, et al.Journal of Voice : Official Journal of the Voice Foundation|October 19, 2010
Voice characteristics in adults with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Paul Corthals, et al.American Journal of Medical Genetics. Part A|November 5, 2011
Objective assessment of nasality in Flemish adults with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.International Journal of Language & Communication Disorders|November 11, 2009
Speech disorders in neurofibromatosis type 1: a sample surveyMarjan Cosyns, Lies Vandeweghe, Geert Mortier, et al.Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|November 23, 2016
Attitudes of European Geneticists Regarding Expanded Carrier ScreeningSandra Janssens, Davit Chokoshvili, Danya Vears, et al.Clinical Dysmorphology|March 15, 2006
Two female siblings with congenital heart disease, postaxial polydactyly, ectopic neuropituitary gland, hair anomalies and characteristic facial features: a new syndrome?Linde Goossens, Sandra Janssens, Valerie Meersschaut, et al.Pageof 8