Melissa Hill
0000-0003-3900-1425
10 papers found
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Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis
Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing
“The communication and support from the health professional is incredibly important”: A qualitative study exploring the processes and practices that support parental decision‐making about postmortem examination
Has Noninvasive Prenatal Testing Impacted Termination of Pregnancy and Live Birth Rates of Infants With Down Syndrome?:
Offering non-invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
Preferences for prenatal diagnosis of sickle-cell disorder: A discrete choice experiment comparing potential service users and health-care providers
Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study
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