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Personalized Medicine
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May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticists
Davit Chokoshvili, Sandra Janssens, Danya Vears, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Barber-Say syndrome in a father and daughter
Nathalie 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 variant
Dorian 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 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Journal of Fluency Disorders
|
September 14, 2010
Word-final prolongations in an adult male with neurofibromatosis type 1
Marjan 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 1
Marjan 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 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
International Journal of Language & Communication Disorders
|
November 11, 2009
Speech disorders in neurofibromatosis type 1: a sample survey
Marjan 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 Screening
Sandra 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.
Page
of 8
Search research articles
Search
Showing results (1-10 of 79) with videos related to
Sort By:
Page
of 8
Personalized Medicine
|
May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticists
Davit Chokoshvili, Sandra Janssens, Danya Vears, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Barber-Say syndrome in a father and daughter
Nathalie 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 variant
Dorian 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 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Journal of Fluency Disorders
|
September 14, 2010
Word-final prolongations in an adult male with neurofibromatosis type 1
Marjan 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 1
Marjan 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 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
International Journal of Language & Communication Disorders
|
November 11, 2009
Speech disorders in neurofibromatosis type 1: a sample survey
Marjan 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 Screening
Sandra 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.
Page
of 8