ACNP - Italian Periodicals Catalogue

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Results: 1-12 |

Results: 12

Screening for foetal malformations: performance of routine ultrasonographyin the population of the Swiss Canton of Vaud

Authors: Vial, Y Tran, C Addor, MC Hohlfeld, P

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

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

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

A characteristic EEG pattern in 4p-syndrome: case report and review of theliterature

Authors: Zankl, A Addor, MC Maeder-Ingvar, M Schorderet, DF

Citation: A. Zankl et al., A characteristic EEG pattern in 4p-syndrome: case report and review of theliterature, EUR J PED, 160(2), 2001, pp. 123-127

An uncommon G375C substitution in a newborn with achondroplasia

Authors: Addor, MC Gudinchet, F Truttmann, A Schorderet, DF

Citation: Mc. Addor et al., An uncommon G375C substitution in a newborn with achondroplasia, GEN COUNSEL, 11(2), 2000, pp. 169-174

Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome

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

Registration of congenital anomalies in Switzerland by EUROCAT (vol 130, pg 1319, 2000)

Authors: Addor, MC Pescia, G Schorderet, DF

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

Untitled

Authors: Ayme, S Addor, MC

Citation: S. Ayme et Mc. Addor, Untitled, SCHW MED WO, 130(38), 2000, pp. 1317-1318

Registration of congenital anomalies in Switzerland by EUROCAT

Authors: Addor, MC Pescia, G Schorderet, DF

Citation: Mc. Addor et al., Registration of congenital anomalies in Switzerland by EUROCAT, SCHW MED WO, 130(38), 2000, pp. 1319-1325

Data on selected malformations in the EUROCAT study

Authors: Achermann, S Addor, MC Schinzel, A

Citation: S. Achermann et al., Data on selected malformations in the EUROCAT study, SCHW MED WO, 130(38), 2000, pp. 1326-1331

Trisomy 21 and its prenatal detection in the Canton of Vaud (1980-1996)

Authors: Pescia, G Addor, MC

Citation: G. Pescia et Mc. Addor, Trisomy 21 and its prenatal detection in the Canton of Vaud (1980-1996), SCHW MED WO, 130(38), 2000, pp. 1332-1338

Turner's syndrome

Authors: Monney, C Pescia, G Addor, MC

Citation: C. Monney et al., Turner's syndrome, SCHW MED WO, 130(38), 2000, pp. 1339-1343

Congenital diaphragmatic hernia: a European population-based study of epidemiology, prenatal diagnosis and mortality

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

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