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Journal of Community Genetics|February 28, 2012
The wide variation of definitions of genetic testing in international recommendations, guidelines and reportsJorge Sequeiros, Milena Paneque, Bárbara Guimarães, et al.Journal of Community Genetics|December 4, 2015
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, JamaicaKarlene Mason, Felicea Gibson, Ruth-Ann Gardner, et al.Journal of Community Genetics|November 27, 2013
Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics servicesSilvana Santos, Anne Aluska da Silva Pequeno, André Pessoa, et al.Journal of Community Genetics|December 25, 2013
"To perpetuate blindness!": attitudes of UK patients with inherited retinal disease towards genetic testingBarbara Potrata, Martin McKibbin, Jennifer Nw Lim, et al.Journal of Community Genetics|February 5, 2016
"It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcareAlison D Archibald, Chriselle L Hickerton, Samantha A Wake, et al.Journal of Community Genetics|February 11, 2016
Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicineColin Me Halverson, Kristin E Clift, Jennifer B McCormickJournal of Community Genetics|May 27, 2016
Swedish healthcare providers' perceptions of preconception expanded carrier screening (ECS)-a qualitative studyA Matar, U Kihlbom, A T HöglundJournal of Community Genetics|November 20, 2017
A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settingsHuma Q Rana, Sarah R Cochrane, Elaine Hiller, et al.Journal of Community Genetics|September 5, 2017
Racial minority group interest in direct-to-consumer genetic testing: findings from the PGen studyLatrice Landry, Daiva Elena Nielsen, Deanna Alexis Carere, et al.Journal of Community Genetics|September 8, 2017
Increasing the involvement of diverse populations in genomics-based health care-lessons from haemoglobinopathiesHelen M RobinsonPageof 82