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European Journal of Human Genetics : EJHG|May 5, 2019
Perspectives in genetic counseling for spinal muscular atrophy in the new therapeutic era: early pre-symptomatic intervention and test in minorsClara Serra-Juhe, Eduardo F TizzanoDiagnostics (Basel, Switzerland)|December 24, 2021
Current Status of Genetic Counselling for Rare Diseases in SpainSara Álvaro-Sánchez, Irene Abreu-Rodríguez, Anna Abulí, et al.European Journal of Human Genetics : EJHG|January 24, 2013
A Delphi study to determine the European core curriculum for Master programmes in genetic counsellingHeather Skirton, Sivia Barnoy, Charlotta Ingvoldstad, et al.European Journal of Human Genetics : EJHG|June 16, 2018
Utility of two SMN1 variants to improve spinal muscular atrophy carrier diagnosis and genetic counsellingLaura Alías, Sara Bernal, Maite Calucho, et al.Journal of Assisted Reproduction and Genetics|May 3, 2026
Integrating preconception carrier screening into public health: lessons learned from a pilot implementation studyAina Marsal-Olivan, Clara Serra-Juhe, Alicia Artigas-Baleri, et al.Journal of Genetic Counseling|November 3, 2020
Beyond the disease itself: A cross-cutting educational initiative for patients and families with rare diseasesEulàlia Rovira-Moreno, Anna Abuli, Marta Codina-Sola, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 22, 2019
Psychiatric genetic counseling: A mapping exerciseRamona Moldovan, Kevin A McGhee, Domenico Coviello, et al.Pageof 1