1. 56 Parent and health professional experiences and views of genome sequencing for rapid diagnosis in critically ill children. (22nd November 2019) Authors: Hill, Melissa; Hammond, Jennifer; Lewis, Celine; Mellis, Rhiannon; Clement, Emma; Chitty, Lyn Journal: Archives of disease in childhood Issue: Volume 104:Supplement 4(2019) Page Start: A23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 69 Looking beyond no primary findings in the 100, 000 genomes project: can additional bioinformatics analysis reveal diagnoses?. (22nd November 2019) Authors: Hay, Eleanor; Morrogh, Deborah; Clement, Emma; Ashton, Emma; Buckton, Andrew; Lombard, Patrick; Faravelli, Francesca; Kumar, Ajith; Hurst, Jane; Chitty, Lyn; Scott, Richard Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 4 Page Start: A27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 97 Exploring health professional attitudes towards rapid fetal exome sequencing for prenatal diagnosis: What do we need to do to ensure safe implementation?. (22nd November 2019) Authors: Mellis, Rhiannon; Hill, Melissa; Chitty, Lyn Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 4 Page Start: A38 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cell-free fetal DNA: emerging applications and future obstacles. (November 2012) Authors: Oxenford, Kerry; Hill, Melissa; Chitty, Lyn Journal: Expert review of obstetrics & gynecology Issue: Volume 7:Number 6(2012) Page Start: 513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Client Views and Attitudes to Non‐Invasive Prenatal Diagnosis for Sickle Cell Disease, Thalassaemia and Cystic Fibrosis. Issue 6 (3rd May 2014) Authors: Hill, Melissa; Compton, Cecilia; Karunaratna, Madhavi; Lewis, Celine; Chitty, Lyn Journal: Journal of genetic counseling Issue: Volume 23:Issue 6(2014) Page Start: 1012 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Development of the Knowledge of Genome Sequencing (KOGS) questionnaire. Issue 11 (November 2018) Authors: Sanderson, Saskia C.; Loe, Bao Sheng; Freeman, Maddie; Gabriel, Camila; Stevenson, Danielle C.; Gibbons, Chris; Chitty, Lyn; Lewis, Celine Journal: Patient education and counseling Issue: Volume 101:Issue 11(2018) Page Start: 1966 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Exploring the impact of Osteogenesis Imperfecta on families: A mixed-methods systematic review. Issue 3 (July 2019) Authors: Hill, Melissa; Lewis, Celine; Riddington, Megan; Crowe, Belinda; DeVile, Catherine; Götherström, Cecilia; Chitty, Lyn Journal: Disability and health journal Issue: Volume 12:Issue 3(2019) Page Start: 340 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Fetal central nervous system anomalies: When should we offer exome sequencing?. (20th April 2022) Authors: Baptiste, Caitlin; Mellis, Rhiannon; Aggarwal, Vimla; Lord, Jenny; Eberhardt, Ruth; Kilby, Mark D.; Maher, Eamonn R.; Wapner, Ronald; Giordano, Jessica; Chitty, Lyn Other Names: Van den Veyver Igna guestEditor. Journal: Prenatal diagnosis Issue: Volume 42:Number 6(2022) Page Start: 736 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Non‐invasive Prenatal Diagnosis for BRCA Mutations – a Qualitative Pilot Study of Health Professionals' Views. Issue 1 (16th July 2015) Authors: Bennett, Jade; Chitty, Lyn; Lewis, Celine Journal: Journal of genetic counseling Issue: Volume 25:Issue 1(2016) Page Start: 198 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32. Issue 12 (1st December 1999) Authors: Lees, Melissa M; Winter, Robin M; Malcolm, Sue; Saal, Howard M; Chitty, Lyn Journal: Journal of medical genetics Issue: Volume 36:Issue 12(1999) Page Start: 888 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗