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Journal of Community Genetics|June 6, 2026
Public and patient involvement in developing a survey on re-consent for pediatric genomic data sharing in Japan: a GRIPP2-LF reportHiroko Terui-Kohbata, Midori Yamamoto, Tomoyo Takeuchi
Journal of Community Genetics|April 12, 2023
Never "totally prepared": Support groups on helping families prepare for a child with a genetic conditionKaitlynn P Craig, Kirsten A Riggan, Sabina Rubeck, et al.
Journal of Community Genetics|August 18, 2023
Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive studyThamires Rosa Dos Santos, Nicoly Stefani Sevalho Carlucci, Lucimar Retto da Silva de Avó, et al.
Journal of Community Genetics|August 15, 2023
Psychosocial impacts of caring for a child with a genetic disorder in Accra, GhanaPaul Opoku, Annabella Osei-Tutu, Mabel Oti-Boadi
Journal of Community Genetics|July 30, 2026
The current state of Spanish language resources for patients in Alabama with rare genetic disease: qualitative expert stakeholder interviewsSpencer Elizabeth Favor, Alicia Gomes, Carlos Javier Torres, et al.
Journal of Community Genetics|July 20, 2026
Carrier screening and genetic counseling in high-consanguinity populations: a narrative reviewAbeer Zakariyah, Babajan Banaganapalli
Journal of Community Genetics|August 10, 2026
Trends in awareness and uptake of genetic testing among the United States population, 2011-2022Ariana Naaseh, Mengyao Shi, Steven Tohmasi, et al.
Journal of Community Genetics|August 19, 2026
Global research trends and influential contributions in sickle cell disease: a bibliometric analysis of the top 100 cited papersSudip Bhattacharya, Alok Singh, Akanksha Singh, et al.
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