Search

Author/Creator McLeod, D R

1. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition. Issue 5 (31st July 2005)

Authors:
Davey, K M; Parboosingh, J S; McLeod, D R; Chan, A; Casey, R; Ferreira, P; Snyder, F F; Bridge, P J; Bernier, F P
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 5(2006)
Page Start:
385
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. Issue 3 (1st March 2002)

Authors:
Baysal, B E; Willett-Brozick, J E; Lawrence, E C; Drovdlic, C M; Savul, S A; McLeod, D R; Yee, H A; Brackmann, D E; Slattery, W H; Myers, E N; Ferrell, R E; Rubinstein, W S
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 3(2002)
Page Start:
178
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search