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Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. [electronic resource] by
- Halford, S
- Wadey, R
- Roberts, C
- Daw, S C
- Whiting, J A
- O'Donnell, H
- Dunham, I
- Bentley, D
- Lindsay, E
- Baldini, A
Producer: 19940331
In:
Human molecular genetics vol. 2
Availability: No items available.
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