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European Journal of Medical Genetics|May 29, 2007
Uncombable hair syndrome: a clinical reportClaudine Rieubland, Pierre A de Viragh, Marie-Claude Addor
Revue Medicale De La Suisse Romande|April 21, 2004
[Epidemiology of lip-maxilla-palate clefts in the canton of Vaud]Marie-Claude Addor, Laurence Feldmeyer, Judith Hohlfeld, et al.
Annales De Genetique|April 2, 2003
Distal trisomy 14 (q24 --> qter) and aorto-pulmonary window: a case report and review of the literatureYannick Perrin, Marie-Claude Addor, Nicole Sekarski, et al.
Pediatric Surgery International|May 23, 2024
Anatomic parameters of omphaloceles and their association with anatomic, genetic, or syndromic malformations: a retrospective studyGallien Parata, Yvan Vial, Marie-Claude Addor, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 5, 2009
Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regionsEster Garne, Maria Loane, Marie-Claude Addor, et al.
Swiss Medical Weekly|December 5, 2014
Evaluation of prenatal diagnosis of congenital heart disease in a regional controlled case studyMarie-Claude Rossier, Yvan Mivelaz, Marie-Claude Addor, et al.
Paediatric and Perinatal Epidemiology|April 30, 2005
Season of birth in valvular heart diseaseDaniela Bosshardt, Vladeta Ajdacic-Gross, Phung Lang, et al.
Congenital Heart Disease|April 2, 2008
Survival and health in liveborn infants with transposition of great arteries--a population-based studyEster Garne, Maria A Loane, Vera Nelen, et al.
Cardiology in the Young|November 28, 2012
Atrioventricular septal defects among infants in Europe: a population-based study of prevalence, associated anomalies, and survivalNikolas Christensen, Helle Andersen, Ester Garne, et al.
Human Mutation|July 21, 2009
Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytesIstván Magyar, Dvora Colman, Eliane Arnold, et al.
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