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Martina Cornelia Cornel

Showing results (1-10 of 8) with videos related to

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Journal of Medical Internet Research|July 17, 2024
Policy Guidance for Direct-to-Consumer Genetic Testing Services: Framework Development StudySuzanne Maria Onstwedder, Marleen Elizabeth Jansen, Martina Cornelia Cornel, et al.
Pediatrics|December 23, 2009
Neonatal screening for treatable and untreatable disorders: prospective parents' opinionsAnne Marie Catharina Plass, Carla Geertruida van El, Toine Pieters, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2006
Developing and optimizing a decisional instrument using self-reported ancestry for carrier screening in a multi-ethnic societyPhillis Lakeman, Lidewij Henneman, Pieter Dirk Bezemer, et al.
Frontiers in Genetics|February 4, 2026
Incidental genomic findings in large scale research: using the "3-I framework" to reveal policy considerationsSuzanne Maria Onstwedder, Carla Van El, Wendy Rodenburg, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?Phillis Lakeman, Anne Marie Catharina Plass, Lidewij Henneman, et al.
Orphanet Journal of Rare Diseases|April 9, 2025
'We are the engine': a focus group study on clinical practice guideline development with European patient advocates for rare congenital malformations and/or intellectual disabilityMirthe Jasmijn Klein Haneveld, Chloé Aymée de Mortier, Anne Hugon, et al.
Orphanet Journal of Rare Diseases|March 15, 2012
Public support for neonatal screening for Pompe disease, a broad-phenotype conditionStephanie Shifra Weinreich, Tessel Rigter, Carla Geertruida van El, et al.
European Journal of Pediatrics|November 9, 2022
Neonatal mortality and morbidity in Down syndrome in the time of prenatal aneuploidy testing: a retrospective cohort studyMaurike Dorothea de Groot-van der Mooren, Brigitta Catharina Scheerman, Lukas Augustinus Johannes Rammeloo, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Medical Internet Research|July 17, 2024
Policy Guidance for Direct-to-Consumer Genetic Testing Services: Framework Development StudySuzanne Maria Onstwedder, Marleen Elizabeth Jansen, Martina Cornelia Cornel, et al.
Pediatrics|December 23, 2009
Neonatal screening for treatable and untreatable disorders: prospective parents' opinionsAnne Marie Catharina Plass, Carla Geertruida van El, Toine Pieters, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2006
Developing and optimizing a decisional instrument using self-reported ancestry for carrier screening in a multi-ethnic societyPhillis Lakeman, Lidewij Henneman, Pieter Dirk Bezemer, et al.
Frontiers in Genetics|February 4, 2026
Incidental genomic findings in large scale research: using the "3-I framework" to reveal policy considerationsSuzanne Maria Onstwedder, Carla Van El, Wendy Rodenburg, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?Phillis Lakeman, Anne Marie Catharina Plass, Lidewij Henneman, et al.
Orphanet Journal of Rare Diseases|April 9, 2025
'We are the engine': a focus group study on clinical practice guideline development with European patient advocates for rare congenital malformations and/or intellectual disabilityMirthe Jasmijn Klein Haneveld, Chloé Aymée de Mortier, Anne Hugon, et al.
Orphanet Journal of Rare Diseases|March 15, 2012
Public support for neonatal screening for Pompe disease, a broad-phenotype conditionStephanie Shifra Weinreich, Tessel Rigter, Carla Geertruida van El, et al.
European Journal of Pediatrics|November 9, 2022
Neonatal mortality and morbidity in Down syndrome in the time of prenatal aneuploidy testing: a retrospective cohort studyMaurike Dorothea de Groot-van der Mooren, Brigitta Catharina Scheerman, Lukas Augustinus Johannes Rammeloo, et al.
Pageof 1