1. Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia. Issue 4 (April 1994) Authors: Zonana, J; Jones, M; Clarke, A; Gault, J; Muller, B; Thomas, N S Journal: Journal of medical genetics Issue: Volume 31:Issue 4(1994) Page Start: 287 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation. Issue 6 (June 1988) Authors: Zonana, J; Roberts, S H; Thomas, N S; Harper, P S Journal: Journal of medical genetics Issue: Volume 25:Issue 6(1988) Page Start: 383 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications. Issue 2 (February 1998) Authors: Ferguson, B M; Thomas, N S; Munoz, F; Morgan, D; Clarke, A; Zonana, J Journal: Journal of medical genetics Issue: Volume 35:Issue 2(1998) Page Start: 112 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗