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Journal of Community Genetics|November 16, 2018
"This could be me": exploring the impact of genetic risk for Huntington's disease young caregiversDanielle S Dondanville, Andrea K Hanson-Kahn, Melinda S Kavanaugh, et al.
Journal of Community Genetics|March 22, 2017
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutationsAisen V Solovyev, Lilya U Dzhemileva, Olga L Posukh, et al.
Journal of Community Genetics|May 14, 2025
Experiences and insights of thalassaemia carriers from an indigenous community in Sabah, MalaysiaNorita Hussein, Yew Kong Lee, Syahirah Mohamed Reza, et al.
Journal of Community Genetics|June 11, 2025
The UK National screening committee, the newborn genomes programme, and the ethical conundrum for UK newborn screeningSara M Rankin, Lucy Marskell, Lina Hamad, et al.
Journal of Community Genetics|January 23, 2026
The effect of sample type on genetic testing completion in pediatric congenital hearing loss patientsBrittany Adams, Lauren Lichten, Aaliyah Heyward, et al.
Journal of Community Genetics|March 26, 2025
Genomics as part of Portuguese undergraduate nursing programs: are we moving in the right direction?Maria João Silva, Maria do Céu Barbieri-Figueiredo, Marcia Van Riper, et al.
Journal of Community Genetics|March 17, 2025
"Hope at a better chance": perspectives on genetic counseling and testing among black individuals with prostate cancerBreanne Prindeville, Brittany M Szymaniak, Samantha E Greenberg, et al.
Journal of Community Genetics|April 11, 2013
The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practiceMartha Driessnack, Sandra Daack-Hirsch, Nancy Downing, et al.
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