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Zankl, A, Addor, MC, Maeder-Ingvar, M and Schorderet, DF (2001) A characteristic EEG pattern in 4p-syndrome: case report and review of the literature. European Journal of Pediatrics, 160 2: 123-127. doi:10.1007/s004310000679 36   15 Cited 19 times in Scopus19 0
Zankl, A, Addor, MC, Gaide, AC, Thonney, F, Cousin, P, Schorderet, DF, Gudinchet, F and Nenadov-Beck, M (2000) Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome. American Journal of Medical Genetics, 95 5: 510-512. doi:10.1002/1096-8628(20001218)95:5<510::AID-AJMG18>3.0.CO;2-V 28   0 0
Zankl, A, Addor, MC and Schorderet, DF (1999). De novo t(3;4)(q21;q31) translocation in an infant with spinal muscular atrophy type I (Werdnig-Hoffmann disease) and no deletion of SMN1.. In: American Journal of Human Genetics. , , (A349-A349). . 16   0
Zankl, A, Addor, MC, Cousin, P, Gaide, AC, Gudinchet, F and Schorderet, DF (2001) Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene. European Journal of Pediatrics, 160 5: 296-299. doi:10.1007/s004310100738 21   9 Cited 12 times in Scopus12 0