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Author/Creator James, Chela

1. An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes. Issue 1 (December 2017)

Authors:
Le Quesne Stabej, Polona; James, Chela; Ocaka, Louise; Tekman, Mehmet; Grunewald, Stephanie; Clement, Emma; Stanescu, Horia; Kleta, Robert; Morrogh, Deborah; Calder, Alistair; Williams, Hywel; Bitner-Glindzicz, Maria
Journal:
Orphanet journal of rare diseases
Issue:
Volume 12:Issue 1(2017)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Circulating tumour DNA sequencing to determine therapeutic response and identify tumour heterogeneity in patients with paediatric solid tumours. (February 2022)

Authors:
Stankunaite, Reda; George, Sally L.; Gallagher, Lewis; Jamal, Sabri; Shaikh, Ridwan; Yuan, Lina; Hughes, Debbie; Proszek, Paula Z.; Carter, Paul; Pietka, Grzegorz; Heide, Timon; James, Chela; Tari, Haider; Lynn, Claire; Jain, Neha; Portela, Laura Rey; Rogers, Tony; Vaidya, Sucheta J.; Chisholm, J...
Journal:
European journal of cancer
Issue:
Volume 162(2022)
Page Start:
209
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Issue 3 (2nd March 2017)

Authors:
Reid, Emma S.; Williams, Hywel; Anderson, Glenn; Benatti, Malika; Chong, Kling; James, Chela; Ocaka, Louise; Hemingway, Cheryl; Little, Daniel; Brown, Richard; Parker, Alasdair; Holden, Simon; Footitt, Emma; Rahman, Shamima; Gissen, Paul; Mills, Philippa B.; Clayton, Peter T.
Journal:
Journal of inherited metabolic disease
Issue:
Volume 40:Issue 3(2017)
Page Start:
385
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗