14 results on '"Chitty, Lyn S."'
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2. Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
3. Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals
4. Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
5. Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges
6. Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study
7. Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta
8. Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study
9. Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management
10. Comparison of diagnostic performance for perinatal and paediatric post-mortem imaging: CT versus MRI
11. Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
12. Lung aeration on post-mortem magnetic resonance imaging is a useful marker of live birth versus stillbirth
13. Postmortem magnetic resonance appearances of congenital high airway obstruction syndrome
14. Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children
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