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L Michaud

Showing results (461-470 of 509) with videos related to

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Nature Genetics|March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndromeDuane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
Frontiers in Public Health|April 28, 2025
Identifying recruitment strategies to improve the reach of evidence-based health promotion, disease prevention, and disease self-management interventions: a scoping reviewPaul A Estabrooks, Mickey L Bolyard, Tallie Casucci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Paediatric and Perinatal Epidemiology|October 27, 2016
3D Cohort Study: The Integrated Research Network in Perinatology of Quebec and Eastern OntarioWilliam D Fraser, Gabriel D Shapiro, François Audibert, et al.
Ebiomedicine|June 9, 2022
The role of common genetic variation in presumed monogenic epilepsiesCiarán Campbell, Costin Leu, Yen-Chen Anne Feng, et al.
Human Mutation|April 28, 2016
Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor ImpairmentMyriam Srour, Véronique Caron, Toni Pearson, et al.
American Journal of Human Genetics|July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Childhood Obesity (Print)|October 29, 2025
Considerations for Cost Assessment of Implementing Family Healthy Weight Programs Across Community and Clinical ContextsTzeyu L Michaud, Jennie L Hill, Kate A Heelan, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Biological Psychiatry|July 22, 2010
De novo truncating mutation in Kinesin 17 associated with schizophreniaJulien Tarabeux, Nathalie Champagne, Edna Brustein, et al.
Pageof 51

Showing results (461-470 of 509) with videos related to

Sort By:
Pageof 51
Nature Genetics|March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndromeDuane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
Frontiers in Public Health|April 28, 2025
Identifying recruitment strategies to improve the reach of evidence-based health promotion, disease prevention, and disease self-management interventions: a scoping reviewPaul A Estabrooks, Mickey L Bolyard, Tallie Casucci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Paediatric and Perinatal Epidemiology|October 27, 2016
3D Cohort Study: The Integrated Research Network in Perinatology of Quebec and Eastern OntarioWilliam D Fraser, Gabriel D Shapiro, François Audibert, et al.
Ebiomedicine|June 9, 2022
The role of common genetic variation in presumed monogenic epilepsiesCiarán Campbell, Costin Leu, Yen-Chen Anne Feng, et al.
Human Mutation|April 28, 2016
Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor ImpairmentMyriam Srour, Véronique Caron, Toni Pearson, et al.
American Journal of Human Genetics|July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Childhood Obesity (Print)|October 29, 2025
Considerations for Cost Assessment of Implementing Family Healthy Weight Programs Across Community and Clinical ContextsTzeyu L Michaud, Jennie L Hill, Kate A Heelan, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Biological Psychiatry|July 22, 2010
De novo truncating mutation in Kinesin 17 associated with schizophreniaJulien Tarabeux, Nathalie Champagne, Edna Brustein, et al.
Pageof 51