1. Spondyloepiphyseal dysplasia tarda: a new autosomal recessive variant with mental retardation. Issue 6 (June 1987) Authors: Kohn, G; Elrayyes, E R; Makadmah, I; Rösler, A; Grünebaum, M Journal: Journal of medical genetics Issue: Volume 24:Issue 6(1987) Page Start: 366 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Issue 11 (November 1992) Authors: Myring, J; Meredith, A L; Harley, H G; Kohn, G; Norbury, G; Harper, P S; Shaw, D J Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 785 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Prenatal diagnosis and gonadal findings in X/XXX mosaicism. Issue 2 (April 1977) Authors: Kohn, G; Cohen, M M; Beyth, Y; Ornoy, A Journal: Journal of medical genetics Issue: Volume 14:Issue 2(1977) Page Start: 120 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗