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Journal of Community Genetics|February 27, 2025
Experiences of stigmatization and its impacts among individuals living with hereditary diseases and family members in Portugal: an exploratory studyJoana Valentim, Milena Paneque, Álvaro MendesJournal of Community Genetics|November 18, 2025
Universal newborn screening for familial hypercholesterolaemia-insights from healthcare professionals in Queensland, AustraliaCaroline Bachmeier, Deborah Johnston, Karam Kostner, et al.Journal of Community Genetics|November 18, 2025
Genetic exceptionalism and genomic contextualism among Asian Americans: a qualitative studySarah D Huang, Daphne Martschenko, Casey R Scherer, et al.Journal of Community Genetics|September 30, 2025
Factors affecting genetic counseling experiences of foreign residents in Japan: implications for healthcare inclusivityKate Nakasato, Moeko Isono, Kazuto KatoJournal of Community Genetics|September 30, 2025
Genetic and genomic insights of the Comcáac peopleAlejandra Paulina Pérez-González, Israel Aguilar-Ordoñez, Norma A Caballero, et al.Journal of Community Genetics|September 25, 2025
From past to progress: a retrospective study on CFTR genetic testing in South AfricaSarah Walters, Colleen Aldous, Helen MalherbeJournal of Community Genetics|November 22, 2022
Telehealth in genetic counselling consultations: the impact of COVID-19 in a Portuguese genetic healthcare serviceMayla A A Dantas, Jorge Diogo Da Silva, Nataliya Tkachenko, et al.Journal of Community Genetics|October 16, 2020
Birth defect mortality in India 1990-2017: estimates from the Global Burden of Disease dataDhammasagar Ujagare, Anita KarJournal of Community Genetics|July 27, 2021
Investigating the reasons for marriage among couples with thalassemia minor, in IranFatemeh Hasanshahi, Narges KhanjaniJournal of Community Genetics|June 6, 2022
Carrier detection probabilities for autosomal recessive variants in unrelated and consanguineous couples - an evaluation of the 86 genes of the ACMG 'Tier 3' panelJörg Schmidtke, Michael KrawczakPageof 82