Citation: Y. Vial et al., Screening for foetal malformations: performance of routine ultrasonographyin the population of the Swiss Canton of Vaud, SWISS MED W, 131(33-34), 2001, pp. 490-494
Authors:
Zankl, A
Addor, MC
Cousin, P
Gaide, AC
Gudinchet, F
Schorderet, DF
Citation: A. Zankl et al., 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, EUR J PED, 160(5), 2001, pp. 296-299
Authors:
Zankl, A
Addor, MC
Gaide, AC
Thonney, F
Cousin, P
Schorderet, DF
Gudinchet, F
Nenadov-Beck, M
Citation: A. Zankl et al., Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome, AM J MED G, 95(5), 2000, pp. 510-512
Citation: Mc. Addor et al., Registration of congenital anomalies in Switzerland by EUROCAT (vol 130, pg 1319, 2000), SCHW MED WO, 130(51-52), 2000, pp. 2026-2026
Authors:
Garne, E
Quataert, P
de Vigan, C
Mendizabal, H
Igoe, D
Addor, MC
Bayon, CM
Garcia-Minaur, S
Lillis, DF
Citation: E. Garne et al., Congenital diaphragmatic hernia: a European population-based study of epidemiology, prenatal diagnosis and mortality, PRENAT N M, 4(6), 1999, pp. 441-447