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Cancers|June 2, 2021
A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene StudyJulie Lapointe, Michel Dorval, Jocelyne Chiquette, et al.Brain : a Journal of Neurology|April 13, 2022
A brain atlas of axonal and synaptic delays based on modelling of cortico-cortical evoked potentialsJean-Didier Lemaréchal, Maciej Jedynak, Lena Trebaul, et al.European Journal of Human Genetics : EJHG|February 16, 2026
Genetic counseling services for hereditary breast and ovarian cancer: patients' experience and satisfaction with different service modelsOuerdia Haroun, Julie Lapointe, Rachel Guérard, et al.Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.Pageof 59