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Author/Creator Firth, H

1. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. Issue 4 (1st April 2004)

Authors:
Shaw-Smith, C; Redon, R; Rickman, L; Rio, M; Willatt, L; Fiegler, H; Firth, H; Sanlaville, D; Winter, R; Colleaux, L; Bobrow, M; Carter, N P
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 4(2004)
Page Start:
241
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome. Issue 4 (1st April 2005)

Authors:
Tatton-Brown, K; Douglas, J; Coleman, K; Baujat, G; Chandler, K; Clarke, A; Collins, A; Davies, S; Faravelli, F; Firth, H; Garrett, C; Hughes, H; Kerr, B; Liebelt, J; Reardon, W; Schaefer, G B; Splitt, M; Temple, I K; Waggoner, D; Weaver, D D
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 4(2005)
Page Start:
307
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗